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

Part of paid clinical trials in Wauwatosa, Wisconsin.

Sponsor
Marquette University
Study ID
NCT05900999
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Feasibility of idle time exercise — BEHAVIORAL
    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.

Study Details

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.

Key Dates

Start date
Nov 29, 2022
Status verified
Oct 2025
Primary completion
Feb 7, 2025
Completion
Oct 3, 2025

Study Design

Enrollment
42 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: Survivors of stroke in early stages of recovery

Primary Outcome Measure

Ratio of Average Activity Duration (RAAD) [ Time Frame: During device use in an inpatient setting (about 1 to 3 weeks of use). ]

Locations (1)

FacilityCityStateZIPSite coordinators
Froedtert Memorial HospitalWauwatosaWisconsin53226-

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