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Telerehabilitation for Multiple Sclerosis

Telerehabilitation for Multiple Sclerosis: Artificial Intelligence vs. Conventional Approaches in Strength Training. A Sin-gle-Blinded Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06871072
Acronym
TRHBN
Enrollment
58
Registered
2025-03-11
Start date
2025-04-01
Completion date
2025-08-31
Last updated
2025-09-19

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

Conditions

Multiple Sclerosis

Keywords

artificial intelligence, exercise, multiple sclerosis, physical therapy, strength, telerehabilitation

Brief summary

Multiple sclerosis (MS) is a neurodegenerative disease affecting the central nervous system and is a leading cause of disability in young adults. It often produces strength deficits. Exercise has been shown to improve strength, mobility, and quality of life while reducing fatigue. Telerehabilitation offers a convenient, accessible alternative for MS patients. This study explores the use of an AI-powered application for prescribing and monitoring strength exercises, ensuring continuous feedback and adherence. Methods: Randomized clinical trial. Intervention of 3 weekly strength training ses-sions for 20 weeks, patients in the experimental group used the AI application, while patients in the control group followed the conventional method, paper-based exercises with access to videos.

Interventions

OTHERTelerehabilitation

EG performed using an artificial intelli-gence (AI) application called RehBody, which detects body segments, assists in cor-recting the technique and monitoring the exercise, number of sets and repetitions done, and the adherence percentage

OTHERExercise program

CG participants followed the exercise program and trained at home with images and videos as support.

Sponsors

University of Cadiz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

Enter the total number of arms participants might be assigned to over the course of the clinical study.

Intervention model description

A neurology will be diagnosed the Multiple sclerosis .

Eligibility

Sex/Gender
ALL
Age
35 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of multiple sclerosis according to the McDonald criteria 2017: * Age between 35 and 60 years. * Score on the Expanded Disability Status Scale in Multiple Sclerosis by Kurtzke (EDSS) between 2 and 6 points. * Patients who do not require assistive devices for home mobility. * Patients with no changes in disease-modifying treatment in the last 3 months. * Patients who have understood, completed, and signed the informed consent and the study information sheet.

Exclusion criteria

* Patients who have been regularly performing strength exercises for more than 3 months prior. * Moderate/severe cognitive impairment that may interfere with the understanding and/or execution of the study. * History of alcohol and/or drug abuse. * Presence of a relapse and/or treatment with corticosteroids within the four weeks prior to the start of the study. * Patients with severe comorbidities other than MS that may pose a risk for following the exercise guidelines or for their participation in the study for other reasons.

Design outcomes

Primary

MeasureTime frameDescription
Maximal StrengthBaselineMaxi-mal Strength was assessed using an 8-repetition maximum test , in which par-ticipants perform 8 repetitions of squat and bench press as the resistance is gradually increased until a load is determined where only eight repetitions can be performed. The load increment was determined based on the result from the Modified Borg Scale at the end of the exercise, if the Borg rating was greater than 7, the test was completed.

Secondary

MeasureTime frameDescription
Maximal Strength.Ten weeks.Maxi-mal Strength was assessed using an 8-repetition maximum test, in which par-ticipants perform 8 repetitions of squat and bench press as the resistance is gradually increased until a load is determined where only eight repetitions can be performed. The load increment was determined based on the result from the Modified Borg Scale at the end of the exercise, if the Borg rating was greater than 7, the test was completed.
Strength endurance.BaselineStrength endurance was measured by the maximum number of unilateral knee flexion-extension repetitions performed in 30 seconds
Endurance capacity.Baseline.Endurance capacity as secondary variable was measured by 6-minutes walking test , where participants covering the maximum distance on a flat surface in 6 minutes. Fatigue was quantified by Modified Fatigue Impact Scale .

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026