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Clinical Trials/CTRI/2025/07/090849
CTRI/2025/07/090849Not ApplicableNot Applicable

Effects of Structural exercise on Community dwelling older adults with Dementia

Dr Ehsanur Rahman1 site in 1 country120 target enrollmentStarted: July 26, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not Applicable
Sponsor
Enrollment
120
Locations
1
Primary Endpoint
1.Dementia Diagnosed by Mini-Mental State Examination (MMSE)

Study Overview

Brief Summary

This randomized controlled trial aims to evaluate the effects of a 12-week structured exercise program on physical and cognitive function in community-dwelling older adults with dementia. Participants will be randomly assigned to either an exercise group receiving strengthening, stretching, and mobility training, or a lifestyle modification group receiving health education and non-physical cognitive/social activities. Primary outcomes include balance, physical function, and daily living ability (MMSE, GDS, FRSSD, SF-36, and Likert Scale -sociodemographic). Secondary outcomes include Physical function (include handgrip test, TUG, BBS, and Chair-Stand Test at baseline, 3 and 6 months).

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
60.00 Year(s) to 95.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Community-dwelling older adults aged 60 years or above; MMSE score of 10 or more; clinically diagnosed dementia with dependence in at least one personal activity of daily living; able to stand up from a chair with armrests with help from one person or less; approved by physician; able to hear and understand instructions for assessments.

Exclusion Criteria

  • Participants will be excluded if they suffer from other neurological disease and severe diseases which would not allow participation in exercise (severe psychiatric illnesses, uncontrolled arterial hypertension, severe cardiorespiratory problems, severe musculoskeletal problems), cancer, surgery during the previous year, severe vision and/or hearing problems, or alcohol and/or drug abuse.

Outcomes

Primary Outcomes

1.Dementia Diagnosed by Mini-Mental State Examination (MMSE)

Time Frame: Baseline at 3 months, 6 months

2. Depression by Geriatric Depression Scale (GDS)

Time Frame: Baseline at 3 months, 6 months

3.Daily living functionality by Functional Rating Scale for Symptoms of Dementia (FRSSD).

Time Frame: Baseline at 3 months, 6 months

4.Quality of life by SF-36 short edition.

Time Frame: Baseline at 3 months, 6 months

5.Likert Scale for sociodemographic question

Time Frame: Baseline at 3 months, 6 months

Secondary Outcomes

  • 1. Physical function assessed by using handgrip test, Timed Up to Go (TUG), Berg Balance Scale (BBS) and Chair-Stand Test (CST)(Baseline at 3 months, 6 months)

Investigators

Sponsor
Dr Ehsanur Rahman
Sponsor Class
Other [university]
Responsible Party
Principal Investigator
Principal Investigator

Al Amin

Jashore University of Science and Technology

Study Sites (1)

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