We will use rates and proportions as appropriate to calculate quantitative feasibility benchmarks. We will also categorize reasons for non-participation, withdrawal, or missed visits. For qualitative feasibility, the unbiased study evaluator will record responses to questions about suitability and acceptability of the intervention. The PI (a trained qualitative investigator) and research staff will use thematic analysis to identify suitability and acceptability of the intervention as well as suggested modifications.43 (link)A plan to maintain participants’ safety and prevent injury has been developed for the study. Occupational therapists are trained to support older adults to safely execute daily activity in the presence of functional limitations. To prevent illness, we will follow CDC recommendations for COVID-19 safety for home health workers, including prophylaxis use and testing as necessary. This research study, all participant education and recruitment materials, and other documents have been approved by the Institutional Review board at the University of Oklahoma health Sciences Center (approval # 14683). This protocol is registered on Clinicaltrials.gov (registration # NCT05600465) This manuscript was prepared using the Standard Protocol Items: Recommendations for Intervention Trials (SPIRIT) Statement, which provides guidance on reporting study protocols. 44 (link) Any modifications to the protocol which impact the conduct of the study will require an amendment to be submitted to the Institutional Review Board and may require approval from the study funder, the Presbyterian Health Foundation. This protocol was submitted for publication 12/21/22, this publication represents version 1 of the protocol.