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NOT YET RECRUITING
NCT07421648
NA

BandPass: A Remote Monitoring System for Sarcopenia and Functional Decline Phase II Aim 4

Sponsor: SynchroHealth LLC

View on ClinicalTrials.gov

Summary

This study evaluates a home-based strengthening program supported by the BandPass system, which includes a Bluetooth-enabled resistance exercise band, a mobile app that provides real-time feedback, and a clinician dashboard for remote monitoring. The goal of this clinical trial is to determine whether older adults living independently can feasibly use the BandPass system and whether participation in a BandPass-guided strengthening program improves functional performance. The main questions this study seeks to answer are: Whether older adults can independently and consistently use the BandPass system as part of a structured home-based strengthening program (feasibility and acceptability). Whether the BandPass-guided program improves functional outcomes, including lower-extremity strength, mobility, and gait performance. Participants will complete a 12-week home strengthening program using the BandPass system, attend in-person and virtual assessment visits to measure strength and mobility, and complete questionnaires related to usability, safety, and overall experience. If successful, this study will provide preliminary evidence supporting the use of remote monitoring technologies to promote strength, mobility, and independence in aging adults and inform the design of future larger-scale trials.

Key Details

Gender

All

Age Range

65 Years - Any

Study Type

INTERVENTIONAL

Enrollment

39

Start Date

2026-02

Completion Date

2026-06

Last Updated

2026-02-19

Healthy Volunteers

No

Interventions

DEVICE

BandPass System

The BandPass system consists of a Bluetooth-enabled resistance exercise band paired with a mobile application that provides real-time feedback on exercise performance and transmits data to a clinician dashboard for remote monitoring. Participants will use the BandPass system for all strengthening sessions during the 8-week intervention.

Locations (2)

UNC Chapel Hill School of Medicine

Chapel Hill, North Carolina, United States

UNC Eastowne Medical Office Building

Chapel Hill, North Carolina, United States