- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04871672
Effects of Pilates Exercises on Core Stability After Recovery From COVID -19
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
145 male and female students who had infected with covid 19 with age 19 to 26 years old, will be recruited from the College of Applied Medical Sciences, Jazan University. Subjects will be randomly assigned to a pilates and home exercises (PAH) group or a control group who will perform only home exercises (COH)
Four core endurance tests will be performed to assess the core stability
Pilates exercise program will be composed of Pilates mat exercise program for a period of 12 weeks and three sessions every week.
Each session took one hour. Every session started with 10 minutes of simple stretching movements to warm-up followed by the main part of the exercise plan for 40 min, followed by 10 minutes, some cool-down stretching.
When the 12-week study period will over, the core stability will be assessed by the endurance tests and Prokin system for balance
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Jazan
-
Riyadh, Jazan, Saudi Arabia, 45142
- Jazan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Persons who had mild to moderate covid- 19 illness.
- Asymptomatic period of at least seven days (without chest pain, breathlessness).
- No musculoskeletal damage.
- No pregnancy.
- No visually identified asymmetries in the spinal trunk and lower limbs.
- None of the subjects has a history of balance training
- Subjects will not have any diseases of the central nervous system.
- Subjects with body mass index (BMI)<25 kg/m2.
Exclusion Criteria:
- Persons who had more severe covid 19 illnesses and were hospitalized.
- Persons who had during their illness chest pain breathlessness, palpitation, symptoms, and signs of heart failure.
9. Subjects with cardiopulmonary disorders. 3. A history of previous back or abdominal surgery/injury 4. Evidence of a systemic or musculoskeletal disease within the past six months
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: pilates and home exercises (PAH) group
these subjects will receive pilates and home exercises.
|
basic five pilates intermediate workout based on the principles of Pilates
home exercise
|
|
Active Comparator: control home exercises group (COH)
these subjects will receive only home exercises.
|
home exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of core stability: endurance capacity of anterior deep trunk muscles
Time Frame: at the date of the first session and at the last session after 12 weeks
|
Abdominal fatigue test: is an isometric trunk flexor test
|
at the date of the first session and at the last session after 12 weeks
|
|
Evaluation of core stability: assesses the functioning of trunk extensor muscles
Time Frame: at the date of the first session and at the last session after 12 weeks
|
Sorensen back-extension endurance
|
at the date of the first session and at the last session after 12 weeks
|
|
Evaluation of core stability: Prone Plank test
Time Frame: at the date of the first session and at the last session after 12 weeks
|
Prone Plank test
|
at the date of the first session and at the last session after 12 weeks
|
|
Evaluation of core stability: Endurance capacity of lateral core muscles particularly the quadrates lumborum
Time Frame: at the date of the first session and at the last session after 12 weeks
|
Side Plank Tests
|
at the date of the first session and at the last session after 12 weeks
|
|
Evaluation of core stability: balance test by Prokin system for perimeter parameter with opened eyes, measured in mm
Time Frame: 30 seconds
|
Eyes Open perimeter (EOPM), measured in mm
|
30 seconds
|
|
Evaluation of core stability: balance test by Prokin system for perimeter parameter with closed eyes, measured in mm
Time Frame: 30 seconds
|
Eyes closed perimeter (ECPM), measured in mm
|
30 seconds
|
|
Evaluation of core stability: balance test by Prokin system for ellipse area parameter with Opened eyes, measured in mm
Time Frame: 30 seconds
|
Eyes Open ellipse area (EOEA) measured in mm2
|
30 seconds
|
|
Evaluation of core stability: balance test by Prokin system for ellipse area parameter with closed eyes, measured in mm
Time Frame: 30 seconds
|
Eyes closed ellipse area (ECEA) measured in mm2
|
30 seconds
|
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
- Sponsor-Investigator:
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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