Skip to content

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

Comparison of Upper Extremity Resistance Exercises as Synchronous Tele and Home Programs in Paraplegic Patients: a Randomized, Controlled, Double-blind Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07115693
Acronym
TELERES-SCI
Enrollment
21
Registered
2025-08-11
Start date
2023-04-15
Completion date
2024-04-15
Last updated
2025-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injury

Brief summary

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.

Interventions

BEHAVIORALTelerehabilitation-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.

BEHAVIORALHome 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.

Sponsors

Hacer Önen Tekin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change in upper extremity muscle strength measured by hand-held dynamometerBaseline and after 6 weeks of interventionMuscle strength of the shoulder flexors, extensors, abductors, and wrist flexors and extensors will be measured bilaterally using a hand-held dynamometer. The outcome is reported in Newtons (N).

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026