Mobile based application for tele-rehabilitation of older adults with primary Insomnia

Not Applicable

• Conditions: Health Condition 1: G89-G99- Other disorders of the nervous system

• Registration Number: CTRI/2022/09/045822
• Lead Sponsor: MGM Institute of Health Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Older adults able to read, hear, understand and follow the visual data and auditory data. Older adults with controlled hypertension and controlled diabetes.

Exclusion Criteria

Older adults with a history or current manifestations of Cardiopulmonary diseases, Stroke, Parkinsonââ?¬•s, Multiple sclerosis, Myasthenia gravis, Neuromuscular diseases, Encephalitis, Amyotrophic lateral sclerosis,

Dementia, Alzheimerââ?¬•s disease, Spinal cord injury, Ataxia, Brain tumors, Cerebral aneurysm, Epilepsy and Seizures, Guillain barre syndrome, Head injuries, Meningitis, Cancer, any Systemic malfunction, Physical disabilities, Spinal disc

herniation or dislocation & fractures will be excluded.

These medical conditions will make it difficult for elderly people to physically operate the mobile based application as well as to read, understand and follow the visual and auditory data.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.The Pittsburgh Sleep Quality Index (PSQI) is an effective instrument used to measure the quality and patterns of sleep in the older adult <br/ ><br> <br/ ><br>2.Polysomnography <br/ ><br> <br/ ><br>3. Development of final version of the mobile applicationTimepoint: The Pittsburgh Sleep Quality Index (PSQI) and Polysomnography : Baseline: 1-4 months and post intervention: 15-18 months <br/ ><br> <br/ ><br>Development of final version of the mobile application: 13-14 month

Secondary Outcome Measures

Name	Time	Method
Knowledge, attitude and belief survey, Timed up and go, 30 seconds chair stand test, Functional reach test, arm curl test,Incontinence Impact Questionnaire (IIQ-7) and Urinary distress short form (UDI-6), chair sit and reach, mini cog scale, 6 minute walk testTimepoint: Knowledge, attitude and belief survey: 1-4 months <br/ ><br> <br/ ><br>Timed up and go, 30 seconds chair stand test, Functional reach test, arm curl test,Incontinence Impact Questionnaire (IIQ-7) and Urinary distress short form (UDI-6), chair sit and reach, mini cog scale, 6 minute walk test: Baseline: 1-4 months, post intervention: 15-18 months <br/ ><br>