Synchronous Tele-Resistance Training to Improve Upper Extremity Function in Patients With Spinal Cord Injury

NCT ID: NCT07115693

Last Updated: 2025-08-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

21 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-15

Study Completion Date

2024-04-15

Brief Summary

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This study investigated the effects of resistive exercises applied with synchronized telerehabilitation on upper extremity functions in patients with SCI who use wheelchairs. A randomized controlled trial included 21 patients with SCI between the ages of between18 and 60. Participants were divided into two groups: the Study Group (n=11) and the Control Group (n=10). Participants in the study group applied resistive exercise with a synchronized telerehabilitation method, while participants in the control group applied a home exercise program. The upper extremity muscle strength of the participants was evaluated with hand-held dynamometer before and after the treatment, physical performance with a 20-meter push test, and physical activity level with Physical Activity Scale for Disabled Individuals.

Detailed Description

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Conditions

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Spinal Cord Injury

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Synchronous Telerehabilitation with Resistance Exercises

Participants received live, video-based supervised resistance training 3x/week for 6 weeks.

Group Type EXPERIMENTAL

Telerehabilitation-Based Resistance Exercise Program

Intervention Type BEHAVIORAL

Participants received synchronous telerehabilitation sessions three times per week for six weeks. Each session lasted 45 minutes and included supervised resistance exercises for upper extremity muscle groups. Exercise bands were chosen based on baseline strength. Pulse oximeters were used to monitor heart rate and oxygen saturation.

Home-Based Exercise Program

Participants followed an unsupervised exercise program at home for 6 weeks.

Group Type ACTIVE_COMPARATOR

Home Exercise Program

Intervention Type BEHAVIORAL

Participants were given a home-based, unsupervised exercise program to follow three times per week for six weeks. The exercises were taught at the beginning, and adherence was monitored using a physical activity diary. No tele-supervision was provided.

Interventions

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Telerehabilitation-Based Resistance Exercise Program

Participants received synchronous telerehabilitation sessions three times per week for six weeks. Each session lasted 45 minutes and included supervised resistance exercises for upper extremity muscle groups. Exercise bands were chosen based on baseline strength. Pulse oximeters were used to monitor heart rate and oxygen saturation.

Intervention Type BEHAVIORAL

Home Exercise Program

Participants were given a home-based, unsupervised exercise program to follow three times per week for six weeks. The exercises were taught at the beginning, and adherence was monitored using a physical activity diary. No tele-supervision was provided.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Aged between 18 and 60 years
* Diagnosed with spinal cord injury classified as ASIA A, B, or C
* Cooperative and able to follow verbal instructions
* Has access to online communication devices
* Partially or fully dependent on a wheelchair
* Sufficient upper extremity strength to operate a wheelchair
* Has not undergone surgery in the past 6 months
* Willing to participate and provided informed consent

Exclusion Criteria

* Unwilling or unmotivated to participate
* Presence of a progressive disease
* Fully bedridden
* Significant cognitive impairment
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hacer Önen Tekin

OTHER

Sponsor Role lead

Responsible Party

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Hacer Önen Tekin

investigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Turkish Spinal Cord Paralytics Association at Hüsnü Ayık Special Care Center

Diyarbakır, Kayapınar, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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IST-FTR-TELERES-SCI-2025

Identifier Type: -

Identifier Source: org_study_id

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