- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06628895
Effect of Modified Poco-Poco Exercise to Frailty Stages, Expression of Global DNA Methylation, GDF15 and Lamin A COP
February 27, 2025 updated by: Universitas Padjadjaran
Effect of Modified Poco-Poco Exercise to Frailty Stages, Expression of Global DNA Methylation, GDF15 and Lamin A COP on Elderly Living On Community in Bandung
The goal of this clinical trial is to know the effect of multicomponent exercise in frail elderly in community to aging hallmarks. The main question[s] it aims to answer are:
- Do global DNA methylation levels change in elderly people in Bandung after receiving modified poco-poco exercise?
- Do GDF15 levels change in elderly people in Bandung after they are given modified poco-poco exercise?
- Do lamin A COP levels change in elderly people in Bandung after they are given modified poco-poco exercise?
- Does the level of frailty in elderly people in Bandung change after they are given modified poco-poco exercise?
Participants will be asked to do flexibility, balance, aerobic and strengthening exercise included in poco-poco modified exercise three times a week for 12 weeks
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The elderly population in West Java Province with the age category of 60-64 years is 1.76 million people.
Experts estimate that 25.2% of the Indonesian population experiences frailty.
Frailty can lead to a variety of worsening health conditions.
The frailty process is thought to stem from the failure of various mechanisms associated with markers of aging.
Markers of aging are divided into three categories: primary, antagonistic and integrative.
Biomarkers representing these three categories are global DNA methylation, GDF15 and Lamin A COP. Multicomponent exercise is the most effective intervention in elderly with frailty.
Elderly people in West Java on average only have an education equivalent to junior high school (SMP), so activities that promote physical activity are better focused on health activities in the community.
The poco-poco exercise that is currently commonly practiced almost fulfills the rules of multicomponent exercise for frailty elderly, but poco-poco exercise does not have a muscle strengthening exercise component, so a modified poco-pcoco exercise was created to fulfill this method.
Study Type
Interventional
Enrollment (Estimated)
17
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Istingadah Desiana, dr, SpKFR, Ger(K), FIPM (USG)
- Phone Number: 62 812 7123 9200
- Email: istingadah.desiana@unpad.ac.id
Study Contact Backup
- Name: William Giovani, dr
- Phone Number: 6281271239200
- Email: williamgiovanni146@gmail.com
Study Locations
-
-
Jawa Barat
-
Bandung, Jawa Barat, Indonesia, 40287
- Recruiting
- Puskesmas Sekejati
-
Contact:
- MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Frailty level is in pre-frailty
- MoCA INA score above 18
- Domicile in Bandung City
- Willing to participate in the study after informed consent
Exclusion Criteria:
- There is a hearing impairment that may prevent the subject from receiving verbal instructions
- There is uncorrected visual impairment
- There are musculoskeletal disorders so that they cannot perform exercise procedures or procedures for measuring research variables
- Subjects received other rehabilitation programs
- Post-stroke with average limb muscle strength below three
- There are diseases that cause impaired cognition such as Alzheimer's disease, traumatic head injury, Parkinson's disease.
- There are severe joint diseases such as osteoarthritis and rheumatoid arthritis that may worsen during exercise or may cause difficulty in carrying out the exercise program.
- Severe cardiovascular disease as assessed by a heart and vascular specialist
- Unable to attend Exercises regularly
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Frail elderly living in community
Adult above 60 years old, frailty level based on Fried frailty phenotype, without having diabetes mellitus and cardiac disease
|
Exercise training that consists of flexibility, aerobic, balance and strengthening regime.
The exercise given three times a week, for 12 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change From Baseline in Level of Global DNA Methylation in 12 Weeks
Time Frame: week 0 and week 12
|
Global DNA Methylation will be measured twice using ...
|
week 0 and week 12
|
|
Change From Baseline in Level of Growth Deficiency Factor (GDF15) in 12 Weeks
Time Frame: week 0 and week 12
|
GDF15 will be measured using blood plasma with Enzyme Linked Immuno Assay (ELISA), expected GDF value that show improvement that it will be decreased
|
week 0 and week 12
|
|
Change From Baseline in Level of Lamin A (Cyclic Osteo Progenitor) COP in 12 Weeks
Time Frame: week 0 and week 12
|
Lamin A COP will be measured with flow cytometry from Peripheral Blood Mononuclear Cells (PBMC), the value that shows improvement has a lesser lamin A COP population
|
week 0 and week 12
|
|
Change From Baseline in Level of Frailty in 12 Weeks
Time Frame: week 0 and week 12
|
Level of Frailty is measured using Fried's Frailty Phenotype with range 1-5 with 5 is the worst level of frailty.
Fried's frailty measured with five components that are unintentional weight loss, muscle weakness, exhaustion on activity, slow gait and low physical activity.
|
week 0 and week 12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Irma R. Defi, DR. Med. Sc, dr, SpKFR, Ger(K), Faculty of Medicine Universitas Padjadjaran
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 15, 2024
Primary Completion (Estimated)
March 15, 2025
Study Completion (Estimated)
April 30, 2025
Study Registration Dates
First Submitted
September 26, 2024
First Submitted That Met QC Criteria
October 3, 2024
First Posted (Actual)
October 8, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 27, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IKFR-202410.01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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