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Self-Determination Theory-informed Occupational Therapy Program to Increase Physical Activ

We will evaluate a novel 8-week telehealth-delivered occupational therapy (OT) program among breast cancer survivors that seeks to promote engagement in aerobic physical activity (PA) and muscle strengthening exercise (MSE). The telehealth-based delivery of this OT program circumvents some barriers to OT access and par

Condition(s)Breast Cancer Survivor
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryWe will evaluate a novel 8-week telehealth-delivered occupational therapy (OT) program among breast cancer survivors that seeks to promote engagement in aerobic physical activity (PA) and muscle strengthening exercise (MSE). The telehealth-based delivery of this OT program circumvents some barriers to OT access and participation (e.g., time burden; distance to OT clinic) among breast cancer survivors- particularly important for Oklahoma given that 33% of residents live in rural areas. Additionally, the focus of this program is to promote the preferred aerobic PA and MSE choices of each individual survivor to increase the likelihood of long-term PA engagement. In turn, participants will be more likely to experience the longer-term benefits associated with PA such as improved physical functi
Who can participateInclusion Criteria: 1. ≥18 years old. 2. Ability to speak/read English. 3. Ability to provide informed consent. 4. Having ever received a histologically confirmed diagnosis of invasive breast carcinoma. 5. Having undergone breast conserving surgery or mastectomy for BC in the last 12 months. 6. Owning a smartphone and/or computer with internet access. 7. Willing to participate in once-weekly telehealth-delivered OT sessions for eight weeks. Exclusion Criteria: 1. Currently undergoing chemotherapy or radiation as primary cancer treatment. 2. Planning or preparing for surgery as primary treatment or as a reconstruction procedure in the next 3 months. 3. Presence of distant metastasis. 4. Reporting a Physical Activity Readiness Questionnaire (2017 PAR-Q+) score that indicates PA may potential
Ages18 Years
SexAll
Lead sponsorUniversity of Oklahoma
LocationsOklahoma City, Oklahoma, United States
Start date2024-11-27
NCT IDNCT06671730
Official listinghttps://clinicaltrials.gov/study/NCT06671730

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