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Table 4 Criteria for successful completion

From: Lifestyle intervention in BRCA1/2 mutation carriers: study protocol for a prospective, randomized, controlled clinical feasibility trial (LIBRE-1 study)

Attendance of 70% of the planned lifestyle intervention events (training sessions and nutrition courses) within the first 3 months

• Conduct of study visit after 1 year

• No withdrawal of informed consent within 1 year

• No new occurrence of any of the exclusion criteria during the first 3 months

 
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Pilot and Feasibility Studies

ISSN: 2055-5784