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A digital decision support system (selfBACK) for improved self-management of low back pain: a pilot study with 6-week follow-up
Pilot and Feasibility Studies volume 6, Article number: 72 (2020)
Abstract
Background
Very few of the publicly available apps directed towards self-management of low back pain (LBP) have been rigorously tested and their theoretical underpinnings seldom described. The selfBACK app was developed in collaboration with end-users and clinicians and its content is supported by best evidence on self-management of LBP. The objectives of this pilot study were to investigate the basis for recruitment and screening procedures for the subsequent randomized controlled trial (RCT), to test the inclusion process in relation to questionnaires and app installation, and finally to investigate the change in primary outcome over time.
Methods
This single-armed pilot study enrolled 51 participants who had sought help for LBP of any duration from primary care (physiotherapy, chiropractic, or general practice) within the past 8 weeks. Participants were screened for eligibility using the PROMIS-Physical-Function-4a questionnaire. Participants were asked to use the selfBACK app for 6 weeks. The app provided weekly tailored self-management plans targeting physical activity, strength and flexibility exercises, and education. The construction of the self-management plans was achieved using case-based reasoning (CBR) methodology to capture and reuse information from previous successful cases. Participants completed the primary outcome pain-related disability (Roland-Morris Disability Questionnaire [RMDQ]) at baseline and 6-week follow-up along with a range of secondary outcomes. Metrics of app use were collected throughout the intervention period.
Results
Follow-up data at 6 weeks was obtained for 43 participants. The recruitment procedures were feasible, and the number needed to screen was acceptable (i.e., 1.6:1). The screening questionnaire was altered during the pilot study. The inclusion process, answering questionnaires and app installation, were feasible. The primary outcome (RMDQ) improved from 8.6 (SD 5.1) at baseline to 5.9 (SD 4.0) at 6-week follow-up (change score 1.8, 95% CI 0.7 to 2.9). Participants spent on average 134 min (range 0–889 min) using the app during the 6-week period.
Conclusion
The recruitment, screening, and inclusion procedures were feasible for the subsequent RCT with a small adjustment. The improvement on the RMDQ from baseline to follow-up was small. Time pattern of app usage varied considerably between the participants.
Trial registration
NCT03697759. Registered on August 10, 2018. https://clinicaltrials.gov/ct2/show/NCT03697759
Background
Self-managing disease, such as chronic illness like low back pain (LBP), is positively affected by receiving social support [1, 2]. Using mHealth applications (apps) to support and reinforce desired self-management behavior has been put forward as a promising way to increase the effectiveness of self-management interventions [3,4,5]. Clinical guidelines for LBP commonly recommend self-management [6,7,8]. Self-management may include several different components, such as self-monitoring of symptoms, physical activity, regular strength/flexibility exercises, and patient education.
Within recent years, the number of mHealth apps has grown substantially [9, 10]. The number of available mHealth apps increased from 153.403 in 2015 to 318.572 in 2017 [10]. Of the available mHealth apps, 60% concerned wellness management, 40% targeted health condition management, with 16% of all mHealth apps being disease specific [10]. Most commonly, mental health and behavioral disorders, diabetes, hypertension, and heart and circulatory conditions were targeted [10,11,12] and only 7% of the disease specific apps targeted musculoskeletal conditions [10]. Despite the worldwide prevalence and impact, apps concerning musculoskeletal disorders are underrepresented. Thus, there is a need for developing evidence-based mHealth apps that support management of musculoskeletal disorders such as LBP. Moreover, such apps should be rigorously tested to document their effectiveness. This will be important for informing end-users and health care professionals about the expected benefit of using such tools.
Very few of the available mHealth apps have been rigorously tested and their theoretical underpinning is most often poorly documented [13, 14]. For example, a recent systematic review identified 61 apps for self-management of LBP and concluded that none of the apps were tested in a randomized controlled trial (RCT) and that the app content in general had low quality [14]. An increase in the number of clinical trials investigating safety and effectiveness of mHealth apps is however evident as 135 trials were registered to utilize medical apps at the trial registry www.clinicaltrials.gov in 2013, increasing to 300 in 2015 [15] and 869 in 2017 [10].
In the selfBACK project, a decision support system (DSS) has been developed to support self-management of LBP [16, 17]. The decision support incorporates evidence-based and tailored recommendations for self-management delivered via an app. Where RCTs aim to evaluate the effectiveness of a given intervention, pilot trials often aim to assess the feasibility of the intervention as well as testing recruitment basis and procedures for the following RCT [18]. The objectives of this pilot study were multiple: to investigate the basis for recruitment and screening procedures for the subsequent RCT, to test the inclusion process in relation to completing questionnaires online and installation of apps, and to investigate the change in primary outcome over time.
Methods
Design
This single-armed pilot study was performed in advance of an RCT. All participants were fully informed of the purpose and allocated to the selfBACK intervention. The study followed an a priori defined protocol that was registered before the recruitment of participants was initiated (NCT03697759). The study is reported in accordance with the CONSORT guideline [18]. Approval for the pilot trial was obtained from the regional Ethics committees in Denmark (S-20182000-24) and Norway (2018/791). Approval from the data protection agency was obtained for Denmark (18/17955) through the University of Southern Denmark. In Norway, this was covered by the Ethics committee approval. This pilot study was a part of the larger selfBACK project funded by the European Union Horizon 2020 research and innovation program (grant agreement no 689043).
Participants
Inclusion and exclusion criteria are described in Table 1.
Recruitment procedure
Recruitment of participants took place in Trondheim, Norway, and Odense, Denmark, from August to November 2019. The flow of the participants throughout the study is shown in Fig. 2 and described in detail elsewhere [19]. People with LBP could be referred to the pilot study after seeing a primary care clinician (i.e., general practitioner, physiotherapist, chiropractor). Additionally, in Denmark, recruitment was also conducted from the Spine Center of Southern Denmark that performs diagnostic assessment of people with back-related problems. Participants identified as potentially eligible by the clinician were given verbal and/or written information about the pilot study by the referring clinician and asked to contact the research team by email or phone or provide their contact information on a sign-up sheet allowing the research team to contact them. Recruitment rates from the different types of primary care providers and the Spine Center were tracked. In addition, experiences concerning the type of communication with clinics and clinicians that were most successful and how to maintain a good contact with the recruiting clinics were discussed during weekly meetings in the research teams, summarized, and considered when planning for the RCT.
Screening procedure
Interested participants were contacted via phone by the research team and screened for eligibility using a standardized screening form with the inclusion and exclusion criteria (Additional file 2). The researchers read the questions aloud from the screening form to participants and recorded their answers. If eligible and willing to participate, the participants gave their verbal consent to participate, received a link to complete a baseline questionnaire, and were invited to a meeting with the researcher. At this meeting, participants received information on the study and gave their written informed consent to participate. The inclusion criterion for mild-to-severe disability was assessed using the PROMIS-Physical Functioning 4 questionnaire (PROMIS-PF4). This is an outcome aiming at measuring disability, which is a recommended core outcome in clinical trials for LBP populations [20]. The questionnaire consists of 4 items asking people with LBP to rate their difficulty performing four activities (chores, stair walking, 15 min walk, running errands) on a 5-point Likert scale ranging from “without any difficulty” to “unable to perform.” Total scores range between 4 and 20 with lower scores indicating more disability. A score of 16 or below was indicative for eligibility.
Intervention
All participants had the selfBACK app installed on their smartphone during a visit with the research team who helped with the app installation and answered any questions that participants might have. Hereafter, participants were asked to use the selfBACK app for 6 weeks to self-manage their LBP in addition to receiving their usual care. The selfBACK app is an add-on to and not a substitution for treatment or seeking advice from HCPs. The development of the selfBACK app, its underlying structure, and development of content have been described in detail elsewhere [16]. In brief, the selfBACK app provides weekly tailored self-management plans targeting three main activities: (1) general physical activity (i.e., number of steps) measured by a step-detecting wristband, (2) strength and flexibility exercises, and (3) patient education (Fig. 1). In addition, the app also provides access to variety of tools and information on management of LBP that the participants could use at their convenience. Examples of tools are a goal-setting tool, mindfulness audios, pain relieving exercises, and general information about the nature of LBP. The feasibility of the app was assessed in a mixed-methods study prior to this pilot study. The results will be reported in a separate publication.
Screenshot of the selfBACK app plan screen showing the three main components of a weekly self-management plan
Demographics and self-reported outcomes
Demographics and self-reported outcomes were collected using a web-based questionnaire. Demographics included gender, age, height/weight (to calculate body mass index [BMI]), civil status and children, education, employment status, and work characteristics. All outcomes were collected at baseline and after 6 weeks (Table 2) using a web-based questionnaire to gauge its feasibility. The self-reported outcomes included the recommended core set of outcomes for LBP trials [20, 38,39,40] (physical functioning, pain intensity, and health-related quality of life). Only results from the primary outcome (Roland-Morris Disability Questionnaire [RMDQ]) will be reported on here, all other scores are given in Additional file 1.
App usage
Participants’ use of the app was tracked using the Matomo software (https://matomo.org/) that registers participants’ time and interactions in the app. The following variables were extracted to illustrate app usage: number of total visits to the app, number of days the app was visited, number of daily visits to the app, total time spent in the app, number of self-management plans generated, and achievements on physical activity, exercises, and education (i.e., percentage completion of the recommendation for each of these activities).
Statistical analysis
Descriptive statistics were used to describe the baseline characteristics of the included participants and the change in the primary outcome from baseline to 6-week follow-up. The baseline characteristics were described as frequencies and means ± standard deviation (SD), the self-reported outcomes were described as means ± SD for baseline and 6-week follow-up, whereas change scores are presented as means with 95% confidence intervals (CI). App usage data is presented as group means and range.
No sample size calculations were performed as this pilot study aimed to investigate the recruitment, screening, and inclusion procedures and to investigate the size of change in score for the primary outcome for the subsequent RCT, rather than to investigate effect or statistical significance of this change from the intervention. The expected sample size for the pilot study was consequently based on feasibility. We aimed to include 70–80 participants (45–60 in Denmark and 15–20 in Norway) within a 3-month recruitment period.
Results
Flow of participants throughout the study is shown in Fig. 2. A total of 93 potential participants consented to be contacted for participation in the pilot study. Of these, we reached 80 potential participants who were assessed for eligibility. After the assessment for eligibility, 51 participants were included.
Flow of the participants throughout the study. LBP low back pain
Participant characteristics
Characteristics of the study sample are presented in Table 3. Overall, the included participants were middle aged (mean age 45.5 years [SD 15.0 years]), slightly overweight (mean BMI 27.2 kg/m2), predominantly female (58%), and living with others (72%). Most participants reported to have had LBP lasting for more than 12 weeks during the current episode (58%) with infrequent use of pain medication (i.e., 55% reported that they never or seldom use pain medication). Furthermore, most of the participants reported to be currently employed in a full-time (59%) or part-time (14%) position.
Primary and secondary outcomes
The RMDQ score, which is the primary outcome in the subsequent RCT, improved 1.8 points over the 6-week intervention period (95% CI − 2.9 to − 0.7) (Table 4). Most secondary outcomes improved significantly from baseline to 6-week follow-up, but the numerical differences were modest (Additional file 1).
App usage
Table 5 shows the app usage during the 6-week intervention period. This included usage of the app content and responding to the weekly tailoring questions to have a new self-management plan created. On average, participants visited the app 65 times during the study period, spent 134 min in the app, and visited the app on 22 of the 42 possible days during the intervention period. However, inter-individual variation in app use was considerable, e.g., total number of visits ranged from 1 to 188 and time spent in the app ranged from 0 to 889 min.
Figure 3 shows a box-plot of the average completion levels for the weekly goals in the tailored self-management plans. Physical activity is shown as percentage completion of the daily step goal (e.g., 130% equals goal achieved plus 30% additional steps). Strength and flexibility exercises are shown as exercise volume (e.g., 100% equals 3 weekly exercise sessions of any duration). Education is shown as the percentage of the suggested educational messages that have been read (e.g., 100% means that all the 7 messages for a week have been read). Overall, participants had high completion rates of the weekly goals across all categories: physical activity, exercise, and education.
Box-plot showing the completion levels for physical activity (i.e., no. of steps), exercise, and education. Physical activity is shown as percentage completion of the daily step goal (e.g., 130% equals goal achieved plus 30% additional steps). Strength and flexibility exercises are shown as exercise volume (e.g., 100% equals 3 weekly exercise sessions of any duration). Education is shown as the percentage of the suggested educational messages that have been read (e.g., 100% means that all the 7 messages for a week have been read)
Recruitment
Table 6 shows the number of participants screened from the different types of primary care clinics and the number needed to screen to include one patient. Overall, most participants were recruited from physiotherapy and chiropractic clinics. The average number needed to screen was 1.6.
Screening
Initially, the inclusion criteria “mild to severe disability due to LBP” was assessed using the PROMIS-PF4 [20, 41,42,43,44]. A cutoff point of 16 or below indicated eligibility. This cutoff point was set as a best guess as no studies using the PROMIS-PF4 on a LBP population was available at the time of the pilot study. During the pilot study, we experienced that many of the screened participants seemed to have pain-related disability but did not fall below the cutoff point. We looked at the first 31 participants included, of those, only nine would have been included if enforcing the cutoff point. Consequently, the cutoff point of 16 or below for the PROMIS-PF4 score was not enforced as cutoff point for inclusion to the study for any of the screened LBP patients. We observed a mismatch between the RMDQ score reported at baseline for participants with the same PROMIS-PF4 score. For example, eight participants had a PROMIS-PF4 score of 20 (no disability), but their RMDQ scores ranged between 0 and 18 (no disability to severe disability). We therefore decided to replace the PROMIS-PF4 with the RMDQ in the screening procedure for assessing disability in the remaining part of the pilot study. This substitution allowed us to assess the feasibility of using the RMDQ as the screening tool on the phone for the subsequent RCT. Overall, using the RMDQ for screening proved feasible, i.e., the time used for screening did not increase compared to the PROMIS-PF4 and it was easy for the potential participants to understand and respond to the questions. For the subsequent RCT, a score of ≥ 6 on the RMDQ was used to indicate eligibility. However, this cutoff point was not enforced in the current study and all patients referred with LBP were included if matching the remaining eligibility criteria.
The standardized screening form listed questions related to the inclusion- and exclusion criteria (Additional file 2). Our experiences when screening participants on the phone resulted in a revision of screening questions on terminal illness, cognitive impairments, and serious mental illness as several participants reacted negatively to the wording of these questions. Consequently, the questions concerning these conditions were reworded and combined with the screening question about physical conditions limiting participation in the intervention (e.g., problems getting down on the floor and up again to perform strength and flexibility exercises). This did not result in any change in the characteristics of the target population, but rather consisted of a clarification to ensure that the potential participants understood the requirements for participating in the intervention. On average, it took about 15 min to screen a participant on the phone.
Data collection and app installation
Sending a link to participants via email to access and complete the web-based questionnaire proved feasible. Participants reported that the length of the questionnaires was acceptable. The sending of emails was automated and easily administered and monitored via an online system. During app installation, a researcher was always present to help with any technical issues or answering questions. For the initial app installations, both technical and research team members attended to observe how participants perceived the installation process. Overall, the app installation worked as expected; however, based on observations in the pilot study, a few explanatory sections were added to the installation manual to be followed in the RCT. On average, the app installation and introduction to the wristband and selfBACK system took about 45 min.
Discussion
The present pilot study confirmed that the recruitment procedure, the app installation procedure, and the data collection of outcomes via a web-questionnaire were feasible. The screening procedure was adjusted during the pilot as the PROMIS-PF4 questionnaire showed to be too restrictive, resulting in exclusion of potentially eligible participants. The intervention resulted in a moderate improvement in pain-related disability assessed by the RMDQ, which serves as the primary outcome in the subsequent RCT. Likewise, most secondary outcomes (e.g., pain intensity, fear-avoidance beliefs, and pain self-efficacy) improved but numerical changes were small. Time pattern of app usage varied considerable between the participants.
The suggested minimal clinically important difference in RMDQ score has been shown to vary according to the level of disability in the target population [21]. A 1–2-point reduction has been suggested to be clinically important in populations with low disability levels [45], while others have suggested that a relative reduction of 30% (regardless of level of disability) indicates a minimal clinically important difference [46]. Thus, the 1.8-point reduction in RMDQ score observed in this pilot study is relatively modest regardless of method for determining the minimal clinically important difference. However, it is important to recognize that this pilot study only assessed the within-group change from baseline to 6-week follow-up. The selfBACK RCT will investigate the effectiveness of the app in addition to usual care using the RMDQ as primary outcome measured at 3 months compared to a control group receiving usual care only.
The pilot study showed that the flow of participants referred to the study varied considerably both between countries, type of clinics and clinicians, and the clinicians response to being prompted to recruit rather than the clinicians professional background or the clinical setting. The average number needed to screen to include one participant was 1.6 but ranged from 1.3 to 1.9 between professions. In the RCT, the inclusion criterion for mild-to-severe disability will be assessed by the RMDQ using a score of ≥ 6 to indicate eligibility. Thus, we expect that the number needed to screen will increase slightly in the RCT. Furthermore, for the RCT, we will make some changes to the screening questions related to the other inclusion/exclusion criteria to increase participants understanding of the requirements for participating. Overall, the procedure for recruiting care-seeking patients with LBP from primary care was considered feasible for the RCT.
The pilot study also aimed to investigate the web-based data collection and app installation process. As a part of this process, members of the technical team attended some of the app installations on the different mobile devices brought by the pilot participants. Here, any questions from the participants concerning technical aspects such as understanding the log-in process, the functionality of the app, and participants’ intuitive responses to interpretation of app content, could be registered by the technical team or researchers and discussed with the participants. This allowed us to assess whether any revisions of the app installation procedure was necessary before carrying out the RCT. The comments did not result in any changes to functionality of the app. However, the explanatory text in the app given to participants during their initial log-in was revised, and additional explanation from the researchers was given to the users during installations. For example, text on how to report on exercise was revised and explanations concerning data handling and security and functionality of the step count and synchronization between wristband and app were elaborated on in the installation process. Overall, the pilot study led to two specific changes for the methods for the RCT; (1) the RMDQ questionnaire substituted the PROMIS-PF4 questionnaire as screening tool, and (2) the explanation of app functionality given to participants during app installations was modified.
Conclusion
Pilot participants engaged with the app on a weekly basis and reported high achievement scores within all three content categories: physical activity, exercise, and education. The procedure for recruiting care-seeking patients with LBP from primary health care was feasible. Screening for eligibility on the phone was feasible but led to a change in choice of screening questionnaire from the PROMIS-PF4 questionnaire to the RMDQ. Collection of primary and secondary outcomes by a web-questionnaire proved feasible. The pilot study is followed by a multinational RCT with a two-armed design investigating the effectiveness of the app in a care-seeking LBP population.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- BIPQ:
-
Brief illness perception questionnaire
- BMI:
-
Body mass index
- CBR:
-
Case-based reasoning
- CI:
-
Confidence intervals
- CONSORT:
-
Consolidated Standards of Reporting Trials
- DSS:
-
Decision support system
- FABQ:
-
Fear avoidance-belief questionnaire
- GPE:
-
Global perceived effect
- LBP:
-
Low back pain
- NRS:
-
Numerical rating scale
- PHQ-8:
-
Patient health questionnaire 8-items
- PSEQ:
-
Pain self-efficacy questionnaire
- PSFS:
-
Patient Specific Function Scale
- PSS:
-
Perceived Stress Scale
- QoL:
-
Quality of life
- RCT:
-
Randomized controlled trial
- RMDQ:
-
Roland-Morris Disability Questionnaire
- SD:
-
Standard deviation
- SGPALS:
-
Saltin-Grimbye Physical Activity Level Scale
- WAI:
-
Work ability index
References
- 1.
Prompuk B, Lertwatthanawilat W, Wonghongkul T, Sucamvang K, Bunmaprasert T. Self-management among adults with chronic low back pain: a causal model. Pacific Rim International Journal of Nursing Research. 2018;22:223–36.
- 2.
Schulman-Green D, Jaser SS, Park C, Whittemore R. A metasynthesis of factors affecting self-management of chronic illness. Journal of advanced nursing. 2016;72:1469–89.
- 3.
Beatty L, Lambert S. A systematic review of internet-based self-help therapeutic interventions to improve distress and disease-control among adults with chronic health conditions. Clin Psychol Rev. 2013;33:609–22.
- 4.
Newman MG, Szkodny LE, Llera SJ, Przeworski A. A review of technology-assisted self-help and minimal contact therapies for anxiety and depression: is human contact necessary for therapeutic efficacy? Clin Psychol Rev. 2011;31:89–103.
- 5.
Newman MG, Szkodny LE, Llera SJ, Przeworski A. A review of technology-assisted self-help and minimal contact therapies for drug and alcohol abuse and smoking addiction: is human contact necessary for therapeutic efficacy? Clin Psychol Rev. 2011;31:178–86.
- 6.
Wong JJ, Cote P, Sutton DA, Randhawa K, Yu H, Varatharajan S, Goldgrub R, Nordin M, Gross DP, Shearer HM, et al. Clinical practice guidelines for the noninvasive management of low back pain: a systematic review by the Ontario Protocol for Traffic Injury Management (OPTIMa) Collaboration. Eur J Pain. 2017;21:201–16.
- 7.
Bernstein IA, Malik Q, Carville S, Ward S. Low back pain and sciatica: summary of NICE guidance. BMJ. 2017;356:i6748.
- 8.
Foster NE, Anema JR, Cherkin D, Chou R, Cohen SP, Gross DP, Ferreira PH, Fritz JM, Koes BW, Peul W, et al. Prevention and treatment of low back pain: evidence, challenges, and promising directions. Lancet. 2018;391:2368–83.
- 9.
Wantland DJ, Portillo CJ, Holzemer WL. Slaughter R. McGhee EM: The effectiveness of web-based vs. non-web-based interventions: a meta-analysis of behavioral change outcomes. J Med Internet Res. 2004;6:e40.
- 10.
Aitken M, Clancy B, Nass D: The growing value of digital health - evidence and impact on human health and the healthcare system. The IQVIA Institute for Human Data Science; 2017.
- 11.
Hood M, Wilson R, Corsica J, Bradley L, Chirinos D, Vivo A. What do we know about mobile applications for diabetes self-management? A review of reviews. J Behav Med. 2016;39:981–94.
- 12.
Alessa T, Hawley MS, Hock ES, de Witte L. Smartphone apps to support self-management of hypertension: review and content analysis. JMIR Mhealth Uhealth. 2019;7:e13645.
- 13.
Nicholl BI, Sandal LF, Stochkendahl MJ, McCallum M, Suresh N, Vasseljen O, Hartvigsen J, Mork PJ, Kjaer P, Sogaard K, Mair FS. Digital support interventions for the self-management of low back pain: a systematic review. J Med Internet Res. 2017;19:e179.
- 14.
Machado GC, Pinheiro MB, Lee H, Ahmed OH, Hendrick P, Williams C, Kamper SJ. Smartphone apps for the self-management of low back pain: a systematic review. Best Pract Res Clin Rheumatol. 2016;30:1098–109.
- 15.
Aitken M, Lyle J. Patient adoption of mHealth - use, evidence and remaining barrieres to mainstream accceptance; 2015.
- 16.
Mork PJ. Bach K, self BC: A decision support system to enhance self-management of low back pain: protocol for the selfBACK project. JMIR Res Protoc. 2018;7:e167.
- 17.
Dineen-Griffin S, Garcia-Cardenas V, Williams K, Benrimoj SI. Helping patients help themselves: a systematic review of self-management support strategies in primary health care practice. PLoS One. 2019;14:e0220116.
- 18.
Eldridge SM, Chan CL, Campbell MJ, Bond CM, Hopewell S, Thabane L. Lancaster GA, group Pc: CONSORT 2010 statement: extension to randomised pilot and feasibility trials. Pilot Feasibility Stud. 2016;2:64.
- 19.
Sandal LF, Stochkendahl MJ, Svendsen MJ, Wood K, Overaas CK, Nordstoga AL, Villumsen M, Rasmussen CDN, Nicholl BI, Cooper K, et al. An app-delivered self-management program for people with low back pain: protocol for the selfBACK randomized controlled trial. JMIR Res Protoc. 2019;8:e14720.
- 20.
Chiarotto A, Boers M, Deyo RA, Buchbinder R, Corbin TP, Costa LOP, Foster NE, Grotle M, Koes BW, Kovacs FM, et al. Core outcome measurement instruments for clinical trials in nonspecific low back pain. Pain. 2018;159:481–95.
- 21.
Roland M, Fairbank J. The Roland-Morris Disability Questionnaire and the Oswestry Disability Questionnaire. Spine (Phila Pa 1976). 2000;25:3115–24.
- 22.
Roland M, Morris R. A study of the natural history of back pain. Part I: development of a reliable and sensitive measure of disability in low-back pain. Spine (Phila Pa 1976). 1983;8:141–4.
- 23.
Roland M, Morris R. A study of the natural history of low-back pain. Part II: development of guidelines for trials of treatment in primary care. Spine (Phila Pa 1976). 1983;8:145–50.
- 24.
Hawker GA, Mian S, Kendzerska T, French M. Measures of adult pain: Visual Analog Scale for Pain (VAS Pain), Numeric Rating Scale for Pain (NRS Pain), McGill Pain Questionnaire (MPQ), Short-Form McGill Pain Questionnaire (SF-MPQ), Chronic Pain Grade Scale (CPGS), Short Form-36 Bodily Pain Scale (SF-36 BPS), and Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP). Arthritis Care Res (Hoboken). 2011;63(Suppl 11):S240–52.
- 25.
Waddell G, Newton M, Henderson I, Somerville D, Main CJ. A Fear-Avoidance Beliefs Questionnaire (FABQ) and the role of fear-avoidance beliefs in chronic low back pain and disability. Pain. 1993;52:157–68.
- 26.
Williamson E. Fear Avoidance Beliefs Questionnaire (FABQ). Aust J Physiother. 2006;52:149.
- 27.
Nicholas MK. Self-efficacy and chronic pain. St. Andrews: In annual conference of the British Psychological Society; 1989.
- 28.
Nicholas MK. The pain self-efficacy questionnaire: taking pain into account. Eur J Pain. 2007;11:153–63.
- 29.
Ahlstrom L, Grimby-Ekman A, Hagberg M, Dellve L. The work ability index and single-item question: associations with sick leave, symptoms, and health--a prospective study of women on long-term sick leave. Scand J Work Environ Health. 2010;36:404–12.
- 30.
Horn KK, Jennings S, Richardson G, Vliet DV, Hefford C, Abbott JH. The patient-specific functional scale: psychometrics, clinimetrics, and application as a clinical outcome measure. J Orthop Sports Phys Ther. 2012;42:30–42.
- 31.
Stratford PW, Kennedy DM, Wainwright AV. Assessing the patient-specific functional scale's ability to detect early recovery following total knee arthroplasty. Phys Ther. 2014;94:838–44.
- 32.
EuroQol G. EuroQol--a new facility for the measurement of health-related quality of life. Health Policy. 1990;16:199–208.
- 33.
Cohen S, Kamarck T, Mermelstein R. A global measure of perceived stress. J Health Soc Behav. 1983;24:385–96.
- 34.
Hallegraeff JM, van der Schans CP, Krijnen WP, de Greef MH. Measurement of acute nonspecific low back pain perception in primary care physical therapy: reliability and validity of the brief illness perception questionnaire. BMC Musculoskelet Disord. 2013;14:53.
- 35.
Grimby G, Borjesson M, Jonsdottir IH, Schnohr P, Thelle DS, Saltin B. The “Saltin-Grimby Physical Activity Level Scale” and its application to health research. Scand J Med Sci Sports. 2015;25(Suppl 4):119–25.
- 36.
Fischer D, Stewart AL, Bloch DA, Lorig K, Laurent D, Holman H. Capturing the patient’s view of change as a clinical outcome measure. JAMA. 1999;282:1157–62.
- 37.
Kamper SJ, Maher CG, Mackay G. Global rating of change scales: a review of strengths and weaknesses and considerations for design. J Man Manip Ther. 2009;17:163–70.
- 38.
Deyo RA, Battie M, Beurskens AJ, Bombardier C, Croft P, Koes B, Malmivaara A, Roland M, Von Korff M, Waddell G. Outcome measures for low back pain research. A proposal for standardized use. Spine (Phila Pa 1976). 1998;23:2003–13.
- 39.
Chiarotto A, Terwee CB, Deyo RA, Boers M, Lin CW, Buchbinder R, Corbin TP, Costa LO, Foster NE, Grotle M, et al. A core outcome set for clinical trials on non-specific low back pain: study protocol for the development of a core domain set. Trials. 2014;15:511.
- 40.
Chiarotto A, Deyo RA, Terwee CB, Boers M, Buchbinder R, Corbin TP, Costa LO, Foster NE, Grotle M, Koes BW, et al. Core outcome domains for clinical trials in non-specific low back pain. Eur Spine J. 2015;24:1127–42.
- 41.
Cella D, Yount S, Rothrock N, Gershon R, Cook K, Reeve B, Ader D, Fries JF, Bruce B, Rose M, Group PC. The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years. Med Care. 2007;45:S3–S11.
- 42.
DeWalt DA, Rothrock N, Yount S, Stone AA, Group PC. Evaluation of item candidates: the PROMIS qualitative item review. Med Care. 2007;45:S12–21.
- 43.
Cella D, Riley W, Stone A, Rothrock N, Reeve B, Yount S, Amtmann D, Bode R, Buysse D, Choi S, et al. The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005-2008. J Clin Epidemiol. 2010;63:1179–94.
- 44.
Licciardone J, Worzer WE, Hartzell MM, Kishino N, Gatchel RJ. An overview of the Patient-Reported Outcomes Measurement Information System (PROMIS) for assessing chronic low back pain patients. Journal of Applied Biobehavioral Research. 2017;22:e12057.
- 45.
Stratford PW, Binkley JM, Riddle DL, Guyatt GH. Sensitivity to change of the Roland-Morris back pain questionnaire: part 1. Phys Ther. 1998;78:1186–96.
- 46.
Jordan K, Dunn KM, Lewis M, Croft P. A minimal clinically important difference was derived for the Roland-Morris Disability Questionnaire for low back pain. J Clin Epidemiol. 2006;59:45–52.
- 47.
Kroenke K, Strine TW, Spitzer RL, Williams JB, Berry JT, Mokdad AH. The PHQ-8 as a measure of current depression in the general population. J Affect Disord. 2009;114:163–73.
Acknowledgements
Not applicable
Funding
The selfBACK project has received funding from the European Union Horizon 2020 research and innovation program under grant agreement no 689043. The funding body supervises the conduct of the overall project, but was not involved in the planning, implementation, and interpretation of the pilot study.
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Affiliations
Contributions
All authors contributed to the design and planning of the pilot. CKØ, ALN, and LFS were involved in recruitment, screening, and data collection. LFS provided a first draft of the manuscript and all authors read and approved the final version of the manuscript. NTNU lead the development of the underlying structure for the database and DSS, RGU (Robert Gordon University) lead the physical activity monitoring, and a private company Trade Expansion developed the mobile app. UoSD, NFA (National Research Centre for the Working Environment), NTNU, GLA (University of Glasgow), and RGU developed the content for the app. UoSD is lead in the planning and conducting of the pilot and RCT. Participants were recruited at NTNU and UoSD. NTNU is leading the overall project.
Corresponding author
Correspondence to Louise Fleng Sandal.
Ethics declarations
Ethics approval and consent to participate
Approval for the pilot trial was obtained from the regional Ethics committees in Denmark (S-20182000-24) and Norway (2018/791). Approval from the data protection agency was obtained for Denmark (18/17955) through the University of Southern Denmark. In Norway, this was covered by the Ethics committee approval. All participants gave verbal and their written informed consent before entering the study.
Consent for publication
Not applicable
Competing interests
The overall aim of the selfBACK project is to develop a digital DSS and mobile app to support participants to self-manage their LBP. The results and experiences from the pilot and RCT will inform the further development of the app, which may be introduced into a commercial market.
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Sandal, L.F., Øverås, C.K., Nordstoga, A.L. et al. A digital decision support system (selfBACK) for improved self-management of low back pain: a pilot study with 6-week follow-up. Pilot Feasibility Stud 6, 72 (2020). https://doi.org/10.1186/s40814-020-00604-2
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Keywords
- Low back pain
- Self-management
- App
- Case-based reasoning
- mHealth
- Recommender system
- Artificial intelligence
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