- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07442942
Effect of Exercise of Shoulder - Pelvic Coupling Pattern on Breathing Using Proprioceptive Technique
Effect of Exercise of Shoulder - Pelvic Coupling Pattern on Breathing and Quality of Life of the Elderly Using Proprioceptive Technique
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Gwangsan-guGwangsan-gu
-
Gwangju, Gwangsan-guGwangsan-gu, South Korea, 62271
- Nambu University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants who were able to communicate adequately
- Participants without any musculoskeletal disorders
- Participants aged 65 years or older
- Participants with a score of 24 or higher on a cognitive function test
Exclusion Criteria:
- Participants who declined to participate in the study
- Participants with an implanted pacemaker
- Participants whose oxygen saturation level was below 90% during the pulmonary function test
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: roprioceptive neuromuscular facilitation scapula-pelvis coupling pattern exercise group
The PNF combination of scapular and pelvic pattern intervention was conducted for 30 minutes per session, three times per week, for four weeks. The PNF combination of scapular and pelvic pattern was applied by combining scapular posterior depression with pelvic anterior elevation, and scapular anterior elevation with pelvic posterior depression. During scapular anterior elevation combined with pelvic posterior depression, the therapist placed their hands on the shoulder joint and acromion, and on the ischial tuberosity to provide resistance. During scapular posterior depression combined with pelvic anterior elevation, resistance was applied by placing the hands on the inferior angle of the scapula and the anterior superior iliac spine. Among the PNF techniques, rhythmic initiation was first used to facilitate movement education and enhance kinesthetic awareness. Afterward, dynamic reversals were applied to promote muscle strengthening in the participants. |
The PNF combination of scapular and pelvic pattern intervention was conducted for 30 minutes per session, three times per week, for four weeks. The PNF combination of scapular and pelvic pattern was applied by combining scapular posterior depression with pelvic anterior elevation, and scapular anterior elevation with pelvic posterior depression. During scapular anterior elevation combined with pelvic posterior depression, the therapist placed their hands on the shoulder joint and acromion, and on the ischial tuberosity to provide resistance. During scapular posterior depression combined with pelvic anterior elevation, resistance was applied by placing the hands on the inferior angle of the scapula and the anterior superior iliac spine. Among the PNF techniques, rhythmic initiation was first used to facilitate movement education and enhance kinesthetic awareness. Afterward, dynamic reversals were applied to promote muscle strengthening in the participants. |
|
Active Comparator: Chest cages expansion exercises group
The chest expansion exercise was performed in a seated upright position. The participant interlocked their fingers behind the head and, during exhalation, brought both elbows together while flexing the trunk muscles. During inhalation, the participant moved the elbows outward while extending the trunk to expand the chest wall. The trunk rotation exercise was performed from the same starting position as the chest expansion exercise. During exhalation, the participant rotated and flexed the trunk, lowering the elbow toward the opposite knee. During inhalation, the participant returned to the starting position. This exercise was performed alternately on both sides. |
The chest expansion exercise was performed in a seated upright position. The participant interlocked their fingers behind the head and, during exhalation, brought both elbows together while flexing the trunk muscles. During inhalation, the participant moved the elbows outward while extending the trunk to expand the chest wall. The trunk rotation exercise was performed from the same starting position as the chest expansion exercise. During exhalation, the participant rotated and flexed the trunk, lowering the elbow toward the opposite knee. During inhalation, the participant returned to the starting position. This exercise was performed alternately on both sides. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pulmonary Function Test
Time Frame: 1 year
|
ulmonary function was measured using a diagnostic spirometer (PONY FX, Italy).
To ensure accurate measurement, sufficient explanation and demonstration were provided so that the participants could fully understand the procedure prior to testing.
For the assessment, participants were seated comfortably in a chair.
To prevent air leakage through the nose, a nose clip was applied, and a personal mouthpiece was held firmly between the teeth with the lips sealed tightly around it.
Forced vital capacity (FVC), forced expiratory volume in one second (FEV1), FEV1/FVC ratio, and peak expiratory flow (PEF) were measured.
Participants were instructed to perform three normal resting breaths, followed by a maximal inhalation.
They were then encouraged to exhale as forcefully and rapidly as possible into the spirometer turbine and to maintain exhalation for 5-6 seconds.
After one demonstration and practice trial, a total of four measurements were performed, and the best value was used for analysis.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chest Cage Expansion Test
Time Frame: 1 year
|
For the chest cage expansion test, the participant was positioned in a supine position with the legs extended and the head and trunk aligned in a straight line. Using a measuring tape, the circumference of the chest was measured horizontally at the level of the xiphoid process and the junction of the body of the sternum. Measurements were taken during maximal inhalation and maximal exhalation while the participant maintained stable breathing, and the values were recorded. Chest cage expansion was calculated as the difference between the measurement at maximal inhalation and the measurement at maximal exhalation. The measurement was performed four times, and the average value was used for data analysis. |
1 year
|
|
Quality of Life Assessment
Time Frame: 1 year
|
Quality of life in the elderly was assessed using the Korean version of the WHOQOL-BREF (Yoo, 2017). The Korean WHOQOL-BREF consists of 24 items related to four domains: physical health, psychological health, social relationships, and environment. Each item is scored on a 5-point Likert scale ranging from 1 "not at all" to 5 "very much". The total score is calculated by summing all items, with a maximum possible score of 120 points. Higher total scores indicate better quality of life. |
1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1041478-2023-HR-023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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