Efficacy of Tele-rehabilitation Intervention on Hand, Cognitive Functions & Depression of Hemiparetic Patients

NCT ID: NCT06997978

Last Updated: 2025-05-31

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-02-01

Study Completion Date

2024-11-20

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Information and communication technologies (ICT) are used in telerehabilitation to deliver rehabilitation treatments to patients in their homes or other locations.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Thirty hemiparetic patients with mild hand dysfunction of both sexes participated in the study (Age range was 45- to 55-year-old); 15 patients in the control group (GB) received a selected hand rehabilitation program, whereas 15 patients in the study group (GA) received telerehabilitation intervention. The 9HPT (Nine-hole peg test), FMUE (Fugl Meyer upper extremity), MOCA (Montreal cognitive assessment scale), REHACOM system, and the BECK DEPRESSION INVENTORY QUESTIONNAIRE were used to evaluate the patients in both groups before and after the treatment program began.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hemiparesis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group A

study group A (n = 15) received the hand rehabilitation program through the Tele-rehabilitation program, a technological device. The rehabilitation was three times a week for a total of twelve weeks (36 sessions) following the conclusion of the rehabilitation program.

Group Type EXPERIMENTAL

Tele-rehabilitation

Intervention Type OTHER

Patients at the Telerehabilitation group are contacted via laptops that have cameras, microphones, and a reliable internet connection. The therapist's laptop camera is positioned so the patient may watch the therapist while the therapist demonstrates the exercises. After the therapist performs the exercise on himself, the patient must see the therapist via a laptop camera and then perform the same activity again.

Hand rehabilitation program

Intervention Type OTHER

1. Free exercises:

1\. Wrist flexion and extension 2. Wrist side movement 3. Thumb flexion and extension 4-Finger opposition 5. Palm up and down
2. Ball exercises:

1. Ball grip
2. Finger flexion
3. Thumb extend
4. The pinch exercise
5. Opposition 6- Side squeeze

7\. Extend out
3. Household exercises

1. Roll movement
2. Wrist curl
3. Extending the wrist
4. Pen exercises

1. Pinch and release
2. Pen spine
5. Exercises with coins

1. Coin drop
2. Coin stacking

Group B

control group B (n = 15) received the same hand rehabilitation program at the physical therapy clinic. The rehabilitation was three times a week for a total of twelve weeks (36 sessions) following the conclusion of the rehabilitation program.

Group Type EXPERIMENTAL

Hand rehabilitation program

Intervention Type OTHER

1. Free exercises:

1\. Wrist flexion and extension 2. Wrist side movement 3. Thumb flexion and extension 4-Finger opposition 5. Palm up and down
2. Ball exercises:

1. Ball grip
2. Finger flexion
3. Thumb extend
4. The pinch exercise
5. Opposition 6- Side squeeze

7\. Extend out
3. Household exercises

1. Roll movement
2. Wrist curl
3. Extending the wrist
4. Pen exercises

1. Pinch and release
2. Pen spine
5. Exercises with coins

1. Coin drop
2. Coin stacking

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Tele-rehabilitation

Patients at the Telerehabilitation group are contacted via laptops that have cameras, microphones, and a reliable internet connection. The therapist's laptop camera is positioned so the patient may watch the therapist while the therapist demonstrates the exercises. After the therapist performs the exercise on himself, the patient must see the therapist via a laptop camera and then perform the same activity again.

Intervention Type OTHER

Hand rehabilitation program

1. Free exercises:

1\. Wrist flexion and extension 2. Wrist side movement 3. Thumb flexion and extension 4-Finger opposition 5. Palm up and down
2. Ball exercises:

1. Ball grip
2. Finger flexion
3. Thumb extend
4. The pinch exercise
5. Opposition 6- Side squeeze

7\. Extend out
3. Household exercises

1. Roll movement
2. Wrist curl
3. Extending the wrist
4. Pen exercises

1. Pinch and release
2. Pen spine
5. Exercises with coins

1. Coin drop
2. Coin stacking

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients between the ages of 45 and 55 were included in this study.
* Both men and women were among the patients. Patients with duration of illness between three to six months.
* According to the modified Ashworth scale (MAS), the patients' hand spasticity ranged from grade 1 to +1.
* The patients had a Fugl Myer upper extremity score of at least nine, indicating mild hand function. On the BECK DEPRESSION INVENTORY questionnaire, the patients' score ranged from 17 to 20 (Borderline clinical depression). Every patient had good vision and hearing.
* The patients successfully filled out the consent form and completed the assigned activities.
* In order to enable video communication while at home, patients need to have at least ten years of education to be able to use a smart device that is connected to the internet, such as a laptop, phone, or tablet.
* In addition to medical care, the patients shouldn't receive any other kind of treatment.
* The patients should be able to communicate and obey commands with ease. - - The patients' MMSE scores were over 21, indicating good cognitive abilities.

Exclusion Criteria

* Individuals with unstable medical conditions, such as unstable angina, symptomatic heart failure, or uncontrolled diabetes mellitus or hypertension. - --- Patients who are unable to utilize the video communication device, have moderate to severe impairment of hand functions, or have any other pathology impacting hand function except stroke.
* Patients who have visual or hearing impairments.
* Patients who have communication issues or who have trouble understanding or obeying instructions.
* Individuals who have seizures or psychological disorders.
* Patients who have not had a stroke but have another illness that impairs cognitive function.
* Individuals who have a history of stroke or other neurological conditions.
Minimum Eligible Age

45 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ahmed Alshimy

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ahmed Alshimy

Assistant professor of Physical Therapy

Responsibility Role SPONSOR_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Al Ryada University for Science and Technology

Sadat, Menoufia, Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

P.T.REC/012/004309

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Unaffected Hand in Hemiplegia
NCT05194501 COMPLETED