Occupational therapy addressing the ability to perform activities of daily living among persons living with chronic conditions: a randomised controlled pilot study of ABLE 2.0
Pilot and Feasibility Studies volume 7, Article number: 122 (2021)
The ABLE intervention was developed to enhance the ability to perform activities of daily living (ADL) tasks among persons living with chronic conditions. ABLE is a generic, home-based, individualised, 8-week occupational therapy intervention program, developed to be delivered in Danish municipalities. In a previous study, the feasibility of ABLE was evaluated in terms of content and delivery. In this pilot study, the remaining feasibility aspects of a randomised controlled trial including (i) trial procedures (recruitment and retention), (ii) randomisation, (iii) adherence to program, (iv) feasibility of additional outcome measurements, and (iv) access to information on usual occupational therapy were evaluated.
The study was conducted in a Danish municipality, using a two-armed parallel randomised controlled design, planning a recruitment strategy including 20 persons living with one/more chronic conditions and experiencing problems performing ADL. The following progression criteria were used to determine if a future full-scale randomised controlled trial was feasible: (i) recruitment (50% met the eligibility criteria) and retention (80%), (ii) randomisation (80% accepted randomisation, procedure was executed as planned), (iii) adherence to program (100% followed the treatment protocol), (iv) outcome measurements (80% of the participants delivered relevantly and fully answered questionnaires), and (v) usual occupational therapy (extraction of needed information was successful).
Due to the COVID-19 pandemic, the study was truncated resulting in limited but sufficient data to answer most of the study questions. (i) Eighteen of 37 eligible persons (48.6%) were recruited; of those treated (n = 6), all remained (100%); (ii) 18 accepted randomisation (100%), and procedure was effective; (iii) ABLE was delivered with adherence (100%); (iv) 92.3–100% of the participants gave relevant and complete answers in two of three questionnaires; and (v) needed information on usual occupational therapy was extractable in seven of nine aspects.
Proceeding to full-scale trial is recommendable; however, a few adjustments on outcome measurements, inclusion criteria and extraction of information on usual occupational therapy are needed.
Key messages regarding feasibility
What uncertainties existed regarding the feasibility? The development of the ABLE intervention program and feasibility aspects related to content and delivery have been addressed in previous studies. This pilot study addressed remaining uncertainties including evaluation of trial procedures (recruitment and randomisation), adherence, access to information on usual occupational therapy and feasibility of additional outcome measurements.
What are the key feasibility findings? The procedures for recruitment and randomisation were feasible; the ABLE intervention program was adherently delivered; and almost all the desired information on usual occupational therapy was accessible. In terms of the feasibility of outcome measurements, the administration of the ADL-Questionnaire (ADL-Q) in this client population was associated with challenges, whereas the Occupational Balance Questionnaire (OBQ11) and Client Weighted Problems questionnaire (CWP) were appropriate.
What are the implications of the feasibility findings for the design of the main study? The study results implied a need for a few adjustments related to inclusion criteria, extraction of information on usual occupational therapy and to the outcome measurements. A full-scale randomised controlled trial is recommended.
The number of persons living with chronic conditions is increasing worldwide. A recent register-based study  has revealed that 65.5% of Danish residents, aged 16 or above, have one or more chronic condition. Several studies provide evidence to support that persons with chronic conditions generally experience problems performing activities of daily living (ADL) tasks [2,3,4,5,6,7,8,9]. This is also reflected in the definition of chronic conditions proposed by Goodman et al.: ‘Conditions that last 1 year or more and require ongoing medical attention and/or limit activities of daily living’ . ADL involve tasks that most people need to perform in their everyday lives, including personal and instrumental ADL tasks . Personal ADL involve basic self-care tasks that are necessary to perform for all people across gender, age, culture and interests. Examples are eating, toileting, grooming and dressing. Instrumental ADL tasks involve more complex household chores, necessary for independent living, including shopping, cooking, cleaning and doing laundry . Addressing ADL task performance problems is a core element in occupational therapy and results from studies indicate that occupational therapy interventions in general may improve ADL ability among older persons with various chronic conditions [13,14,15,16]. However, rigorous studies, testing the outcomes of occupational therapy for persons living with chronic conditions experiencing ADL task performance problems are limited [13,14,15,16,17]. A scoping review on occupational therapy for chronic conditions  suggested that similar interventions addressing ADL may be applicable across a range of diagnoses. In support of this, a study examining self-reported quality of ADL task performance among n = 593 persons living with chronic conditions [18, 19], found similar types of ADL task performance problems across a range of chronic conditions. Hence, there was a need to develop a generic intervention program to address decreased ADL ability across chronic conditions causing disability.
Accordingly, the research program “A better everyday life”, launched in 2015, aims to develop and evaluate an occupational therapy intervention program (named ABLE) focusing on enhancing the ADL ability among persons living with chronic conditions experiencing ADL task performance problems. The research program is guided by the British Medical Research Council’s (MRC) guidance on how to develop and evaluate complex interventions . The guidance prescribes four stages: (1) Development, (2) Feasibility/piloting, (3) Evaluation, and (4) Implementation .
In prior phases, the first version of the ABLE intervention program (ABLE 1.0) was developed [18, 19, 21] incorporating knowledge based on existing evidence, clinical expertise of occupational therapists (OTs) and client needs [18, 19, 21, 22]. Moreover, feasibility was addressed in terms of content and delivery, and the selected outcome measurements were ascertained . However, the feasibility evaluation also revealed a need to adjust the recruitment procedure, apply minor changes to the intervention manual and further monitor adherence to the intervention program . A pilot randomised controlled trial (RCT) study was recommended before proceeding to a full-scale RCT .
Consequently, the ABLE intervention program faced pilot testing involving evaluation of trial procedures (including recruitment and randomisation), adherence, feasibility of additional outcome measurements and access to information on usual occupational therapy. In preparation for this, a new strategy for recruitment was planned, a randomisation procedure was developed, the ABLE intervention program manual was revised (ABLE 2.0), questions related to evaluating the feasibility of additional outcome measurements were developed and decisions regarding needed information on usual occupational therapy were made.
Aims and objectives
The overall aim of this ABLE pilot study was to inform the decision on whether to proceed to full-scale RCT. The pilot study should strengthen the design and conduct a future RCT, in relation to the remaining feasibility aspects [24, 25]. The specific aims of the ABLE pilot study were to:
Assess effectiveness of the recruitment process and retention in the context of a future trial
Assess the randomisation procedure and determine the acceptability of randomisation among the participants
Assess adherence to intervention program in the same context as the future RCT trial
Assess appropriateness of additional outcome measurements
Determine if needed information on usual occupational therapy can be extracted from the client records in the municipality
The ABLE pilot was designed as a two-armed parallel randomised controlled study with random and stratified allocation to ABLE 2.0 and usual occupational therapy, respectively (n = 20).
Setting, participants and recruitment
The ABLE pilot study was scheduled to be conducted from January to May 2020 in a Danish municipality, with almost 90,000 inhabitants. The Rehabilitation Unit in the municipality is organised in four comparable geographic areas (North, East, South, and West). Participants were recruited from all four areas. ABLE 2.0 and usual occupational therapy sessions were delivered, and data collection was conducted, in the homes of the participants. Participants in both the ABLE intervention group and the control group (usual occupational therapy) received other health care services as usual.
Eligible participants lived with one or more medically diagnosed chronic condition, were aged ≥ 18 years; lived in own home; experienced ADL task performance problems; communicated independently and relevantly (without severe cognitive deficits); were motivated and ready for making changes in performance of ADL; motivated and ready for cooperating with an occupational therapist (OT) in finding solutions to the experienced problems; and able to understand and relevantly answer a questionnaire. Exclusion criteria were known substance abuse; mental illness and/or other acute illness effecting ADL task performance; or language barriers.
OTs delivering ABLE 2.0 (ABLE OTs) (n = 3) were recruited among OTs in the municipality based on having at least 2 years of experience working with persons living with chronic conditions and ADL task performance problems, and being calibrated as Assessment of Motor and Process Skills (AMPS) [26, 27] raters. In preparation for delivering ABLE 2.0, the ABLE OTs participated in a three-and-a-half-day tailored workshop.
Assessors (n = 2), conducting observation-based outcomes evaluation of ADL ability using the AMPS at baseline and post-intervention, were OTs trained and calibrated as AMPS raters recruited from a nearby Hospital Unit.
Participants were recruited using a two-step model. In the first step, all persons referred to rehabilitation services in the municipality, or persons already receiving any kind of rehabilitation services, were screened for eligibility. A key OT in each Rehabilitation Unit area performed the screening based on a guideline including a checklist on the eligibility criteria. In a telephone conversation, the key OT provided the potential participant with initial information on the ABLE pilot study and asked for permission to forward contact information to the primary investigator. In the second step, and within three weekdays from the forwarded contact information, the primary investigator called to provide more detailed information, determine if the person was interested in participating and finalise screening of eligibility for inclusion. If the person met the inclusion criteria, preliminary oral consent to participate was obtained.
ABLE 2.0 intervention program
The manualised ABLE 2.0 intervention program is a generic, systematic and client-centred 8-week occupational therapy intervention program, addressing ADL task performance problems among persons living with chronic conditions. It is characterised by offering an individualised combination of intervention components adapted to the single person. Three models underpin the ABLE intervention program, namely the Occupational Therapy Intervention Process Model (OTIPM) , describing the problem-solving process (here using an adaptational approach); the Person-Environment-Occupation (PEO) model , here explaining performance of daily activities as doing shaped by the interaction between person, environment and occupation; and finally, the Transactional Model of Occupation (TMO) , clarifying reasons for ADL task performance problems. ABLE 2.0 consists of five to eight sessions (Fig. 1).
Session 1 involves standardised assessment of perceived and observed ADL ability by means of the ADL-Interview (ADL-I)  and the Assessment of Motor and Process Skills (AMPS) [26, 27], respectively. AMPS is an observation-based assessment measuring two aspects of ADL task performance: ADL motor ability (reflecting physical effort) and ADL process ability (reflecting efficiency, safety and independence) [26, 27].
Sessions 3–7 are intervention sessions, focusing on adaptation by employing a combination of intervention components to improve ADL task performance, and delivered face-to-face or by telephone, with or without homework (e.g. practicing strategies and trying out new ways of doing) between sessions.
The final session includes re-evaluation of self-reported and observed ADL ability using the ADL-I and AMPS and evaluation of goal attainment using GAS.
Mandatory sessions are 1–2, and at least two intervention sessions and the final session. The program is delivered in the homes or local areas of the participants and is designed to be implemented as part of community-based rehabilitation. Structure and overall content of ABLE 2.0, including a brief case example, is presented in Fig. 1; Table 2 provides information on the intervention components; and Additional file 1 provides description of instruments and tools used in the ABLE 2.0.
Usual occupational therapy
Participants in the control group received standard occupational therapy services provided by the municipality (usual occupational therapy). To gain a preliminary insight into the usual occupational therapy prior to the pilot study, information was extracted from ten records representing people similar to those to be recruited for the pilot study. Those data suggested that the typical dose of usual occupational therapy was 3 x 60 min. Also, the content of usual occupational therapy seemed to vary based on client conditions and needs, but observation of ADL task performance, counselling and evaluation of the use of helping aids were common. Examples of established goals included “ability to bath independently” or “toilet safety”.
Criteria for progressing to full-scale RCT, based on data derived from this pilot study, were clarified using frameworks by O’Cathain , Bowen  and Charlesworth  and included the following aspects: Recruitment and retention, randomisation procedure, adherence to program, appropriateness of outcome measurements, and information on usual occupational therapy.
Recruitment and retention
The previous feasibility study  revealed recruitment and retention challenges. Thus, 33% of the participants dropped out due to lack of motivation or reporting no need of intervention. Consequently, recruitment procedures in this pilot study were specified to recruit participants that actually experienced ADL task performance problems and were ready to make changes, using a two-step model, described above. Moreover, the former inclusion criteria on motivation and readiness for change were specified by splitting it into two criteria: (a) ‘motivated and ready for making changes in performance of ADL’ and (b) ‘motivated and ready for cooperating with OT in finding solutions to the experienced problems’.
To monitor recruitment and retention, the flow of participants was registered, capturing information on (1) how many persons were contacted to recruit 20 participants for the pilot study, (2) reasons for accepting/not accepting to participate and (3) number of and reasons for dropouts. Progression criteria on recruitment were that 50% of the persons contacted met the eligibility criteria and accepted participation and that 80% stayed in the program.
To assess the randomisation procedure and determine the acceptability of randomisation among the participants, a randomisation procedure was developed reflecting a procedure to be employed in a future randomised controlled trial. Hence, before inclusion of participants, a randomisation list was generated based on permuted random blocks of variable size (2 to 6 in each block). Participants were allocated in a 1:1 ratio to either ABLE or usual occupational therapy taking into account baseline level of observed ADL ability, using AMPS ADL motor ability (≤ 1.0 vs > 1.0) and ADL process ability (≤ 0.7 vs > 0.7) independence cut-offs . Potential participants were informed about randomisation procedures and given the possibility to withdraw. Monitoring method was to register the randomisation progress including reasons to refuse randomisation. Progression criteria were that 80% accepted randomisation and that procedures were executed as planned.
Adherent delivery of ABLE 2.0
Changes to the ABLE manual
The previous feasibility study  revealed some deviations from the manual in delivery (e.g. omission of AMPS in first and/or final sessions, omission of goal setting due to participants having no goals to address, and delivery of less than the minimum of five sessions). Thus, steps were taken to increase adherence to the ABLE manual. The manual was revised, applying results from the feasibility study and also incorporating updates of the theoretical framework OTIPM  underpinning the intervention. To examine the revised ABLE manual in terms of any aspect that could lead to confusion or misunderstanding among OTs delivering the program, a cognitive debriefing  was conducted. The input and suggestions from the participating OTs (n = 5) were incorporated in the manual, resulting in ABLE 2.0. Further details on the cognitive debriefing process will be published in a separate paper.
Changes in training workshop
The training workshop for the ABLE OTs was extended to three-and-a-half days over a period of a month and providing in-between feedback on e.g. the OTs’ use of instruments and delivery of sessions. The workshop consisted of introduction to ABLE 2.0 including underlying intervention theories, practicing the use of instruments, and training delivery of the ABLE intervention components. It was emphasised why both initial AMPS evaluation and goal setting are regarded core mechanisms of change in the program.
Changes in physical environments
The ABLE feasibility study  reported limited access to helping aids to try out and practice using. Accordingly, direct access to helping aids was ensured in the pilot study.
To monitor adherence, registration forms were filled in after each session by both participant and OT informing on perceived engagement; participant involvement, meaningfulness and satisfaction with intervention. Furthermore, OT registration forms informed on number of sessions delivered and time use in each session (dose). Also, what was delivered, including deviations from manual, goal setting and instruments applied for evaluation of ADL ability (fidelity); confidence in delivering the program; unintended side effects; and practical and/or organizational facilitators and barriers. Aspects related to confidence in delivering the program; involvement of participant; OT’s and participant’s engagement, meaningfulness and satisfaction with the program, were scored using Likert scales from 1 to 5; 1 = very low degree, 2 = low degree, 3 = fair degree, 4 = high degree and 5 = very high degree. Progression criterion on adherence was ABLE 2.0 delivered as intended in terms of dose and fidelity.
Appropriateness of outcome measurements
Several outcome measurements planned for application in the full-scale ABLE RCT were already evaluated for appropriateness in the feasibility study , but some remained to be tested: ADL-Questionnaire (ADL-Q) , Occupational Balance Questionnaire (OBQ11) , and five questions specifically constructed for this study, named Client Weighted Problems questionnaire (CWP) (Additional file 2). Appropriateness was evaluated by counting the number of relevantly and fully answered ADL-Q, OBQ11 and CWP questionnaires at baseline and post-intervention. Progression criterion was 80% of the participants giving relevant and complete answers in questionnaires.
ADL-Q is a standardised evaluation tool to describe and measure self-reported quality of ADL task performance , in terms of physical effort and/or fatigue, efficiency, safety and independence. The persons report their perceived ADL ability for each of 47 ADL tasks using seven response categories: (a) I perform the task independently without use of extra time or effort and without risk; (b) I perform the task independently, but I use helping aids; (c) I perform the task independently, but it takes me extra time; (d) I perform the task independently, but I use extra effort/get tired; (e) I perform the task independently, but there is a risk that I might injure myself; (f) I need assistance from someone but do participate; and (g) the task is performed by others for me—I cannot participate actively. The person is instructed to use more than one response category, if several apply to their performance of the specific ADL task (e.g. mark both c and d if they spend extra time and get tired). Finally, ratings for personal ADL tasks should be based on ADL task performances within the past 24 h and for instrumental ADL tasks within the past 7 days .
To create an overall linear measure of self-reported quality of ADL task performance (reported in log-odds probability units; logits), based on the Rasch measurement methods, the mark given in the lowest response category on each task is re-scored using an ordinal rating scale from 0 to 3: Competent (score = 3) covering response categories (a) and (b), Using extra time/effort (score = 2) covering response categories (c) and (d), At risk/need help (score = 1) covering response categories (e) and (f) and Unable (score = 0) covering response category (g) . The present version of the ADL-Q can also be used to measure the person’s perceived satisfaction with the quality of performance for each of the 47 ADL tasks, using a four-point ordinal satisfaction scale: 4 = ‘very satisfied’, 3 = ‘satisfied’, 2 = ‘dissatisfied’ and 1 = ‘very dissatisfied’ . ADL-Q satisfaction measures are also generated based on the Rasch measurement methods . ADL-Q performance measures have demonstrated sensitivity to change, when applied in persons with rheumatoid arthritis .
Occupational Balance Questionnaire
OBQ is an 11-item questionnaire evaluating occupational balance of individuals and groups. Occupational balance is defined as “the experience of having the right amount of occupations and the right variation between occupations, including work, leisure, rest and sleep” . In OBQ11, the participants report their perceived occupational balance for each of 11 items, using a four-response category scale from 0 = ‘completely disagree’ to 3 = ‘completely agree’. Scores are summed into a total score ranging from 0 to 33, with 33 representing complete occupational balance. OBQ11 has been examined for internal construct validity in a general population using the Rasch measurement theory , but not yet in clinical samples.
To complete the investigation on how, from the participants’ point of view, engagement in ADL task performance contribute to well-being, and how the participants experienced changes, five questions (CWP) (Additional file 2) were constructed specifically for this study, e.g.: “How big a problem is it for you, that your chronic condition(s) affects your possibilities to perform and participate in daily tasks in and around your home (e.g. shopping, cleaning, doing laundry, transport)?”. The questions were related to the participant’s identified problems and perceived need for help and hopes for the future. The perceived weight was scored on an 11-point numeric scale ranging from ‘0’ representing “not at all” to ‘10’ representing “to a high extent”.
Accessible information on usual occupational therapy
Decisions on needed information on usual occupational therapy was structured by the MRC guidance , and inspired by Erlen et al.  and Hoffmann et al. . Identification of the specific aspects of information was guided by several hypotheses on mechanisms of action in the ABLE 2.0 intervention program. Aspects included dose (duration of intervention, number of visits, length of visits), evaluation of ADL ability (use of standardised instruments, self-report and/or observation), goal setting (whether goals were formulated, how goals were negotiated), content of treatment phase (applied approaches including practicing performance of ADL tasks, counselling, focus on occupation/body functions/environment, involvement of home carer or relative), referral services (e.g. social services, group exercises or peer support groups) and programmatic and/or clinical changes during trial (changes applied based on e.g. new guidelines or participation in specialised courses) .
The monitoring method was the investigation of routinely collected records of participants receiving usual occupational therapy in the ABLE pilot (n = 10). A study-specific schedule for registering data on the predefined aspects of information was developed. Data collection was conducted by the primary investigator and a person from the municipal Rehabilitation Unit, specialised in client records and knowledgeable about rehabilitation practices in the municipality, but not otherwise involved in the study . Progression criterion was access to information on the predefined aspects of usual occupational therapy in 80% of the participants.
Following inclusion, a letter was sent to the participants, containing written information on the ABLE pilot study, informed consent form and questionnaires. A baseline home visit by an assessor was scheduled within seven weekdays from the inclusion and oral consent. At the visit, the participant was asked to hand in the signed informed consent form and the filled-in questionnaires. If the participant needed help to fill in any of these, the assessor offered and registered the need of help. Thereafter, observation-based evaluation of ADL ability using the AMPS [26, 27] was performed.
To minimise contamination between interventionists, ABLE 2.0 was delivered by OTs employed in Rehabilitation Unit areas West and East, whereas usual occupational therapy was delivered by OTs employed in Rehabilitation Unit areas South and North. The OTs had rare contact across areas, and ABLE OTs were informed not to share information of any kind on ABLE 2.0 with their colleges. Furthermore, the OTs delivering ABLE 2.0 did not deliver usual occupational therapy. Still, to be able to randomise at an individual level, both the ABLE OTs and the usual occupational therapy OTs delivered interventions in all four geographical areas, depending on the outcome of the randomisation.
External assessors were masked on allocation to intervention at post-intervention and follow-up.
Based on the study aims, sample size calculation was not required [42, 43]. Rather, the number of participants was based on representativity related to the target study population, and a sample size large enough to provide useful information about the aspects of the study . Hence, it was decided to include 20 participants.
Data were analysed using IBM SPSS Statistics, version 25. Nominal and ordinal data were reported as number and percentage. Continuous variables were reported as mean and standard deviation (SD), provided that data were normally distributed. Ordinal data and data with lack of normal distribution were presented based on median and range, and nominal data based on percentages. Participant demographic data on age, gender, diagnosis, civic status, job situation, educational level, ADL ability, occupational balance and self-reported general health were presented in a table.
Recruitment, retention and randomisation
Data on recruitment and retention, including number of participants recruited and retention rate, and on randomisation procedures, including flow of participants in relation to randomisation, were presented in flowcharts.
Adherent delivery of ABLE 2.0
Data in registration forms concerning what and how much was delivered, deviations from the intervention manual, work on goal setting, evaluation of ADL ability, unintended side effects and practical and/or organizational facilitators and barriers were summarised and presented in a table, and supported by quotes presented in text.
Appropriateness of outcome measurements
Number of relevantly and fully answered ADL-Q, OBQ11 and CWP questionnaires were reported in numbers and percentages.
Accessible information on usual occupational therapy
Overview on whether information on predefined aspects of usual occupational therapy was accessible or not was provided in a table. Furthermore, it was described if the quality of the information related to goal setting and content of usual occupational therapy was sufficient to be compared to similar types of information gathered during the ABLE intervention.
The COVID-19 pandemic
Due to the COVID-19 pandemic, the ABLE pilot study was truncated on March 12th, 2020. Consequently, an evaluation was performed to determine the extent to which the collected data was sufficient to address the study aims. Additional actions were launched where possible. Data related to monitoring recruitment and randomisation procedures were judged to be sufficient. Information on retention was limited, and rates could not be determined. Data on adherence to program was limited with no opportunity to gather further data. Thus, results of adherence to intervention program was based on information from registration forms related to two completed and three interrupted ABLE interventions. Data on appropriateness of outcome measurements was limited, based on baseline evaluations of 13 participants. Due to the limited data, a supplementary group interview with assessors on their experiences from baseline assessments was conducted. As the number of baseline ADL-Q data was insufficient for generating ADL-Q measures, they could not be reported. Results of information on usual occupational therapy were based on three completed cases. Therefore, information from client records on another seven clients, representative for the study sample and receiving usual occupational therapy interventions before the pilot study, were included. Despite the truncation of the study, it was concluded that the pilot data were sufficient to answer the majority of the study questions.
Presentation of sample
Participant demographic data are presented in Table 1.
A total of n = 37 persons with chronic conditions were assessed for eligibility, and n = 18 were enrolled. Demographic data indicated variation across diagnoses, age, gender, civic status and educational level. Baseline mean AMPS ADL motor ability measures were below competence cut-off (< 2.0 logits) in both the ABLE and usual occupational therapy group, indicating physical effort, fatigue and/or clumsiness during ADL task performance. Also, baseline mean AMPS ADL process ability measures were below competence cut-off (< 1.0 logit), suggesting ineffective use of time, space and objects, safety risk and potential need for assistance in everyday life [26, 27].
Below, results are presented in relation to the specific aims of the pilot study.
Recruitment and retention
Of 37 potential participants contacted, 18 agreed to participate, resulting in an inclusion of 48.6%. Of these, 13 participants went through baseline evaluations before study was truncated (Fig. 2). Seven of the 13 participants needed help filling out the questionnaires. One participant had a limited use of the scale on ADL-Q performance (a score of 6 in 45 of 47 items). She explained her scores by saying: “I can perform all tasks, but I tend to not get it done”. Thus, even though she received daily assistance from spouse to initiate her task performances, she rated her ability to perform the tasks as independent and competent. Furthermore, on the CWP questionnaire she reversed her answers completely, when the assessor gave her further information on the scale.
In relation to retention, no participants dropped out of the study during the active data collection period.
None of the 18 eligible participants refused randomisation. In five cases, further procedures were interrupted due to the COVID-19 pandemic causing lockdown in the municipality. Hence, 13 participants were randomised, with six participants allocated to the ABLE arm and seven to usual occupational therapy arm. All 13 participants stayed in their allocated program until the lockdown (Fig. 2).
Adherent delivery of ABLE 2.0
Sessions delivered, instruments applied, intervention components implemented, and time used
Two participants completed ABLE 2.0 with a minimum of five sessions, and one participant completed ABLE 2.0 except the final session. Another participant completed sessions 1 and 2. In all four cases, evaluation of ADL ability (AMPS and ADL-I) was conducted, and GAS was used for negotiating and setting goals in accordance with the manual. One more participant completed session 1 and went through ADL evaluations (Fig. 2). Finally, one randomised participant did not receive any sessions, before study ending. The two participants completing ABLE 2.0, also went through ADL re-evaluation (AMPS and ADL-I) in the final session as prescribed in the manual.
Eight of the nine potential intervention components to be applied during sessions 3–7 were applied across participants receiving ABLE 2.0 (Table 2).
The median number of minutes spent at sessions delivered face-to-face varied between 27 and 135 minutes with a tendency to spend more time on the first (median = 93 min) and final sessions (median = 72 min) involving ADL evaluations.
In the usual occupational therapy group, three participants completed their intervention process. Another participant had the intervention process interrupted after one visit, and three participants did not enter the usual occupational therapy intervention.
Deviations from the manual
The OTs reported no deviations from the manual, only adjustments within the inherent flexibility of the program. Instruments and models were applied according to the manual.
Goals were negotiated for all participants completing session 2 (n = 4). Two participants each defined two goals, and two participants each defined one goal. The OTs’ satisfaction with delivering session 2 was high (median = 4.5; range: 3 to 5), whereas the OTs experience on how the dialogue on goal setting worked was somewhat lower (median = 3; range: 2 to 5) (Table 3).
The OTs perceived some challenges related to goal setting: “difficult to guide the participant on grading the goals”; “participant found it difficult to understand the scale”; and “it was difficult to explain GAS”. Still, the participants all reported that they highly appreciated working with goal setting (median = 4).
Confidence, engagement, involvement of participant, meaningfulness and satisfaction with ABLE 2.0
The OTs’ confidence in delivering ABLE 2.0 was high, and they felt highly engaged during the sessions (Table 3). Degree of participant involvement was high, with similar scores from OTs and participants. Participants and OTs found the content of the sessions highly meaningful and satisfactory.
Unintended side effects
OTs registrated a few examples of positive side effects: “Based on the ADL task performance during the session, the participant was more able to describe the experienced problem related to the task”; “the participant seemed more motivated [at the end of session 2]”.
Practical and/or organizational facilitators and barriers
There were no registrations of problems related to access to needed helping aids.
Appropriateness of outcome measurements
At baseline, four participants (30.7%) completed the performance ratings of the ADL-Q. In contrast, only two participants (15.4%) completed the satisfaction ratings of the ADL-Q. The OBQ11 assessments at baseline was completed by twelve participants (92.3%). Finally, all participants (100%) completed the CWP questionnaire at baseline. Thus, the progression criterion of 80% completely answered questionnaires was met in OBQ11 and CWP, but not in ADL-Q.
Seven participants needed assistance to fill in the questionnaires, one due to limited vision, another six for reasons like “lack of overview”, “overwhelming”, “lack of energy”, “receiving the questionnaires only the day before the meeting [baseline assessment]” and “not understanding a term [occupational balance]”. Two of these seven participants needing help filling in the questionnaires, received only minor assistance (less than 10% of the items) to complete.
Information on usual occupational therapy
Table 4 presents information on which of the predefined aspects of usual occupational therapy information was accessible.
The quality of the information related to goal setting and content of usual occupational therapy was assessed to be sufficient for comparison to similar types of information gathered during the ABLE intervention.
This pilot study evaluated the remaining feasibility aspects of the ABLE 2.0 intervention program in terms of design, conduct and processes of an outcome trial, including recruitment, randomisation, adherence, appropriateness of outcome measurements and access to information on usual occupational therapy. The results indicated that the procedures for recruitment and randomisation were feasible and that ABLE 2.0 was delivered according to the manual and with engagement. OTs were overall satisfied delivering the ABLE intervention. Moreover, adherence was sufficient since the minimum number of sessions, the mandatory assessments and intervention components for good quality of ABLE 2.0 intervention delivery, were applied by the OTs. Additionally, it was possible to extract almost all the desired information on usual occupational therapy from the client records. Concerning the outcome measurements, the application of ADL-Q in this client population was associated with challenges, whereas the OBQ11 and CWP were eligible.
The revised procedures on recruitment enabled inclusion, as almost half of the persons referred agreed to participate. This differs from the results of the former feasibility study , suggesting the revised procedures are recommendable in a future trial. Considering the challenges related to answering the questionnaires, and the inclusion criteria on ‘being able to understand and relevantly answer a questionnaire’, we recognise that we are dealing with a population that might be challenged on this criterion. Striving at recruiting persons who seem to match the aims of the intervention and a sample as less biased as possible , it is suggested to reduce the amount of questionnaires rather than exclude persons being on the edge of this criteria. Furthermore, we suggest asking potential future participants if they feel confident in answering questionnaires.
In this study, one person, referred for the study, needed help filling in the questionnaires due to limited vision, and another two persons, referred, could not be provided with information on the study due to limited hearing. Hence, their sensory losses introduced a risk to quality of data, preventing them from participation in the study. Accordingly, the exclusion criteria on ‘language barriers’ should be adjusted to ‘communication barriers’. Another three persons, referred, were not included due to lack of motivation. The legislation in Denmark prescribes that persons, who apply for home care to assist with household chores, instead as a standard procedure are referred to reablement, a time-limited intervention provided in people’s homes to support reacquisition of skills to manage their household chores . Being referred to intervention rather than receiving the requested home care, may have resulted in a higher number of potential participants at entrance of the pilot study, who not all were motivated for participating in the program. Furthermore, research indicate that elderly persons who are frail and have decreased health are more difficult to recruit into research [44, 46], as reflected in the progression criteria of 50% on recruitment in this pilot study. Knowing that differences between participants and non-participants might bias the results of a future RCT and decrease external validity , much attention should be paid on recruitment in a future trial.
The challenges on adherent delivery of the first version of ABLE intervention program revealed in the ABLE feasibility study was related to application of AMPS and goal setting. In the present study involving ABLE 2.0, all instruments were applied according to the manual, and only few adjustments were made delivering the sessions, all within the frame of the program. The results indicate that the revisions of the manual and the tailored course for the OTs overall were efficient. In addition, it is appropriate to emphasise, with reference to the MRC’s guidance , that some flexibility in the intervention program should be allowed, as interventions may work better if adaptation is acceptable. Thus, the inherent flexibility in ABLE 2.0 is regarded a strength. Results of the present pilot study related to dose (sessions delivered, intervention components implemented and time use) was quite in line with the positive results from the ABLE feasibility study on the same aspects. Hence, the minimum of five sessions should be maintained.
The biggest challenge on outcome measurements in the ABLE 2.0 pilot was related to answering the ADL-Q performance and satisfaction scales, as only 4 of 13 scored the performance scale, and two of 13 scored the satisfaction scale. Fortunately, we learned from the former feasibility study  that the interview-based equivalent, ADL-I, is feasible in this population. Hence, the use of ADL-I seems more appropriate to use in this population as it likely provides more complete datasets. Previous research has shown that measures of ADL ability is dependent on the methods applied with questionnaire and interview yielding different but related information about ADL ability . The pattern is a higher self-reported ADL ability based on questionnaire compared with interview . Thus, it is recommended to replace the ADL-Q with the ADL-I, evaluating self-reported ADL ability in terms of performance and satisfaction in a future trial. Furthermore, this will ease the participants´ burden related to answering questionnaires.
Thorough information on usual occupational therapy is critical for investigating effectiveness of the ABLE 2.0 intervention program [20, 41, 48]. Hoffmann et al.  suggest describing usual care in a trial with the same level of detail as in the intervention group. But usual care is by nature a dynamic phenomenon. Therefore, it is unlikely that all participants in a control group will receive the same usual care, and furthermore, usual care typically reflects locally adapted practices and may vary at different time points during a trial [40, 49]. Hence, description of usual occupational therapy, based on retrospective investigation on what was delivered to participants receiving usual occupational therapy, should be optimal in a future trial. Information on actual duration of each visit could be requested documented in a future RCT, providing data that are comparable to information gathered during the ABLE intervention. Due to lack of accessibility to information on programmatic and/or clinical changes in the client records in the municipality, it is recommended to conduct short and focused interviews on this aspect, with OTs delivering usual occupational therapy, after the intervention period in a future RCT. Also, it is recommended that data collection on usual occupational therapy is conducted by research staff assisted by a person from the Rehabilitation Unit in the municipality, familiar with clinical practice and client records, to extract information on all possible aspects. Finally, it is recommended to maintain the study-specific schedule developed for this pilot, to collect consistent data on usual occupational therapy interventions.
This pilot study has provided useful information on important aspects related to evaluating the ABLE 2.0 intervention program. Adding the results of this study to the results of the previous feasibility study, and following the recommendations of the MRC guidance on developing and evaluating complex health interventions, progressing to a full-scale RCT including evaluation of effectiveness, processes and economy of the ABLE 2.0 program is recommendable. A limitation of the study is the incomplete dataset, caused by the COVID-19 pandemic prematurely terminating the study and resulting in weaker evidence on some pilot aspects, primarily on adherence to ABLE 2.0 and appropriateness of outcome measurements. There are important findings though, that the procedures on recruitment and randomisation were effective and that it was possible to recruit a sample representing the population being target group of the ABLE intervention. Further, for planning a future trial, it is important to know that the ABLE intervention was delivered according to the manual and that the first five persons included completed the intervention sessions and stayed in the program.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Activities of daily living
A Better everyday LifE
Medical Research Council
Randomised controlled trial
Assessment of Motor and Process Skills
Occupational Therapy Intervention Process Model
Goal Attainment Scaling
Activities of Daily Living Questionnaire
Activities of Daily Living Interview
Occupational Balance Questionnaire
MOS 36-Item Short Form Survey Instrument
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First, we thank all pilot study participants for contributing. We also thank the involved health professionals, in the municipality of Herning for contributing to the study, and the Department of Occupational Therapy and Physiotherapy in the Regional Hospital West Jutland for contributing to the data collection.
This work was funded by: The Oak Foundation [OCAY-13-309]; The municipal fund for quality development [A327]; VIA University College; Southern Denmark University; Bispebjerg and Frederiksberg Hospital, University of Copenhagen; Research Fund of the Danish Association of Occupational Therapy [FF1/19-R112-A2271 and FF2/19-R132-A2835]; and the Lundbeck foundation [A8059].
Ethics approval and consent to participate
The study was approved by the Danish Data Protection Service Agency: Journal-nr. P-2020-203. The Ethical Committee confirmed that no approval was needed for this study: Journal-nr.: 19045758. Informed consent was obtained.
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Hagelskjær, V., Nielsen, K.T., von Bülow, C. et al. Occupational therapy addressing the ability to perform activities of daily living among persons living with chronic conditions: a randomised controlled pilot study of ABLE 2.0. Pilot Feasibility Stud 7, 122 (2021). https://doi.org/10.1186/s40814-021-00861-9