Cognitive Training on Sleeping Disorders in Stroke

NCT ID: NCT05170386

Last Updated: 2025-01-14

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

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-01

Study Completion Date

2024-09-30

Brief Summary

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Cognitive impairment and sleeping disturbance following stroke diagnosis are common symptoms that significantly affect the quality of life.

Detailed Description

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40 patients from both sexes will participate in this study. All the patients have to be diagnosed as stroke patients. The patients will be divided into two groups; group A (20 patients): which will receive cognitive training combined with instructive conventional treatment for a sleeping disorder, and group B (20 patients): which will receive instructive conventional treatment for sleeping disorder all the patients will be assessed pre and post-treatment using 1- Epworth sleeping scale, 2-Pittsburgh sleep quality index ( PSQI) 3- MINI mental cognitive scale

Conditions

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Stroke Sleep Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

group A (20 patients): that will receive cognitive training combined with instructive conventional treatment for sleeping disorder, and group B (20 patients): that will receive instructive conventional treatment for sleeping disorder
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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study group

receive cognitive training combined with instructive conventional treatment for sleeping disorder

Group Type EXPERIMENTAL

Cognitive training Therapy

Intervention Type OTHER

Cognitive training Therapy include: Writing the reminiscences

• Solving a table• Writing a letter making a calendar and writing a note about the daily activities on it Facing patients' fears instead of avoiding them.Using role-playing to prepare for potentially problematic interactions with others.Learning to calm one's mind and relax one's body.

instructive conventional treatment

Intervention Type OTHER

instructive conventional treatment breathing relaxation exercise inform of diaphragmatic breathing Practice sleep hygiene such as keeping a regular sleep schedule. Get regular exercise. Minimize noise. Minimize light. Manage the temperature so that you're comfortable.

control group

receive instructive conventional treatment for sleeping disorder

Group Type EXPERIMENTAL

instructive conventional treatment

Intervention Type OTHER

instructive conventional treatment breathing relaxation exercise inform of diaphragmatic breathing Practice sleep hygiene such as keeping a regular sleep schedule. Get regular exercise. Minimize noise. Minimize light. Manage the temperature so that you're comfortable.

Interventions

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Cognitive training Therapy

Cognitive training Therapy include: Writing the reminiscences

• Solving a table• Writing a letter making a calendar and writing a note about the daily activities on it Facing patients' fears instead of avoiding them.Using role-playing to prepare for potentially problematic interactions with others.Learning to calm one's mind and relax one's body.

Intervention Type OTHER

instructive conventional treatment

instructive conventional treatment breathing relaxation exercise inform of diaphragmatic breathing Practice sleep hygiene such as keeping a regular sleep schedule. Get regular exercise. Minimize noise. Minimize light. Manage the temperature so that you're comfortable.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* stroke onset at least 5 months prior to study enrolment
* with sleeping disturbance
* age will range from 40:55
* upper extremity spasticity ranging from
* according to Modified Ashowrth Scale.

Exclusion Criteria

* difficulty to communicate
* other neurological conditions that cause sleeping disorders
* severe depression or other psychiatric symptoms.
Minimum Eligible Age

40 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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October 6 University

OTHER

Sponsor Role lead

Responsible Party

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Lama Saad El-Din Mahmoud

Lecturer of physical therapy, Department of Neuromuscular disorders and its surgery, faculty of physical therapy, october 6 univerisity

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Lama S Mahmoud

Al Jīzah, Select State, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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P.T. REC/012/003445

Identifier Type: -

Identifier Source: org_study_id

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