Effects of Core Stability Training Using Pilates on Core Muscle Strength, Pulmonary Function, and Cardio-respiratory Fitness in the Elderly.
PLT-AER-ELD
2 other identifiers
interventional
29
1 country
1
Brief Summary
This study investigates how different types of exercise-specifically Mat Pilates and Aerobic training-can help improve the physical health and breathing capacity of healthy older adults aged 60 to 77. As we age, our bodies naturally experience a decline in core strength and lung function, which can make daily activities more tiring. The goal of this research is to compare whether the specialized breathing and core-strengthening techniques of Pilates provide better results for respiratory health and physical endurance than traditional treadmill walking. Study Structure A total of 29 participants from Nakhon Si Thammarat, Thailand, were randomly assigned to one of three groups: Pilates Group: Practicing Mat Pilates sessions focused on core stability and controlled breathing. Aerobic Group: Performing moderate-intensity treadmill walking. Control Group: Maintaining their normal daily routine without a structured exercise program. Duration \& Intensity Both exercise groups trained for 60 minutes, three times a week, over an 8-week period. By comparing these groups, the study aims to identify effective exercise options that can help seniors maintain their independence and improve their quality of life.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2025
CompletedFirst Submitted
Initial submission to the registry
March 8, 2026
CompletedFirst Posted
Study publicly available on registry
March 13, 2026
CompletedMarch 13, 2026
March 1, 2026
7 months
March 8, 2026
March 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Core Stability (Prone Bridge Test)
The total time that the participant can maintain a neutral spine position during the Prone Bridge (Plank) Test. This measures the endurance of the core stabilizing muscles. Unit of Measure: Seconds
Baseline (Week 0) and Post-intervention (Week 8).
Secondary Outcomes (8)
Forced Vital Capacity (FVC)
Baseline (Week 0) and Post-intervention (Week 8)
Forced Expiratory Volume in 1 Second (FEV1)
Baseline (Week 0) and Post-intervention (Week 8)
FEV1/FVC Ratio
Baseline (Week 0) and Post-intervention (Week 8)
Forced Expiratory Flow at 25-75% (FEF25-75%)
Baseline (Week 0) and Post-intervention (Week 8)
Maximum Voluntary Ventilation (MVV)
Baseline (Week 0) and Post-intervention (Week 8)
- +3 more secondary outcomes
Study Arms (3)
Pilates Training Group (PTG)
EXPERIMENTALParticipants receive an 8-week Mat Pilates program (60 mins, 3 times/week) focused on core stability and breathing mechanics.
Aerobic Training Group (ATG)
ACTIVE COMPARATORParticipants perform moderate-intensity treadmill walking (60 mins, 3 times/week) at 55%-70% Heart Rate Reserve.
Control Group (CON)
NO INTERVENTIONParticipants maintain their usual lifestyle and daily activities without any new structured exercise program.
Interventions
A structured 8-week intervention involving 60-minute group sessions, 3 times weekly. Includes 10-minute warm-up, 40-minute Mat Pilates (core activation, limb coordination, and lateral breathing), and 10-minute cool-down. Intensity: 55%-70% HRR.
An 8-week aerobic program consisting of 60-minute treadmill sessions, 3 times weekly. Includes 10-minute warm-up, 40-minute moderate-intensity walking at 55%-70% HRR, and 10-minute cool-down.
Eligibility Criteria
You may qualify if:
- Healthy older adults aged 60-77 years.
- Non-smokers.
- Capable of independent movement and daily activities.
- Not engaged in any structured exercise program for at least 6 months prior to enrollment.
- Free from dietary supplementation for at least 6 months.
- Controlled hypertension (120-159/80-99 mmHg) with physician clearance.
- Willing to provide written informed consent.
You may not qualify if:
- Severe cardiovascular or respiratory diseases.
- Acute or chronic musculoskeletal conditions (e.g., spondylolisthesis, scoliosis, arthritis, or gout).
- Severe back pain or tendinitis that hinders exercise.
- Uncontrolled hypertension.
- Use of medications that significantly affect heart rate or physical performance.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Walailak Universitylead
- Chulalongkorn Universitycollaborator
Study Sites (1)
School of Medicine, Walailak University
Nakhon Si Thammarat, Changwat Nakhon Si Thammarat, 80160, Thailand
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Bulin Jirapongsatorn, Master degree
School of Medicine, Walailak University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Participants and instructors could not be blinded due to the nature of exercise interventions. However, the outcome assessors and data analysts were blinded to the group assignments.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 8, 2026
First Posted
March 13, 2026
Study Start
September 1, 2024
Primary Completion
March 15, 2025
Study Completion
March 31, 2025
Last Updated
March 13, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
To protect the privacy and confidentiality of the participants, individual participant data will not be made publicly available. However, the study protocol and statistical analysis plan may be shared upon reasonable request to the Principal Investigator.