CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 42 enrolled
Drug / intervention
Feasibility of idle time exercisebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05900999
NCT05900999N/ACompleted

Addressing Arm Non-use by Encouraging Idle-time Activity During Early Recovery From Stroke

Marquette University·interventional·Posted Jun 13, 2023·Updated Jan 16, 2026

In Brief

A clinical study evaluating Feasibility of idle time exercise for Stroke and Exercise. Completed, enrolled 42 participants across 1 site.

Detailed Summary

This project evaluates the feasibility of using custom wearable technology and associated procedures to increase activity of the more-involved upper extremity during the earliest stages of recovery from stroke by increasing the amount of therapeutic exercise during idle-time. The proposed research is relevant to public health because it takes steps to mitigate a significant problem in physical rehabilitation using low-cost technology to motivate and monitor idle-time exercise without adding significantly to clinician workloads. The project aligns with the NICHD / NCMRR Research Plan on Rehabilitation by exploiting a mobile health (mHealth) and sensor-based approach to promote health and wellness through participant-engaged, data-driven, individualized care.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsStroke, Exercise
CountriesUnited States

Timeline

N/ACompletedFinished
2023202420252026
First PostedJun 13, 2023
Enrollment StartNov 29, 2022
Primary CompletionFeb 7, 2025
Study CompletionOct 3, 2025
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 3.1 years ago

Interventions

Feasibility of idle time exercisebehavioral

The experiments in this proposal will assess the utility and subjective patient experience performing idle time exercise intervention designed to reduce learned non-use of the hemiparetic arm in the days, and weeks immediately following stroke. Exercise will be cued by wearable technology that provides vibrotactile cues similar to those provided by FitBit devices. Participants will be asked to perform simple exercises after receiving a vibration cue. In the first four sessions they will tap the more-involved wrist; in the second four sessions they will passively move the more-involved elbow through a range of motion; in the final four sessions they will actively move the more-involved elbow through a range of motion. Accelerometers in the wearable devices will monitor motion of the wrist during the exercise sessions. We will interview the participants two months later regarding how well they use the more-involved arm to perform daily activities.