- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06471725
Effectiveness of Adding Pilates Exercises to Sports Hernia Rehabilitation:a Comparative Clinical Trial (PESHR)
June 18, 2024 updated by: Hany Mohamed Ibrahim Elgohary, Cairo University
The study recruited male sports hernias patients referred for physical therapy by an orthopedist or general practitioner from Damietta General Hospital.
Participants had to be between 18 and 45 years old, have had sports hernia for two to ten weeks, and be willing and able to attend and stick to the Pilates exercise program for the trial's entire duration
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The study recruited male sports hernias patients referred for physical therapy by an orthopedist or general practitioner from Damietta General Hospital.
Participants had to be between 18 and 45 years old, have had sports hernias for two to ten weeks, and be willing and able to attend and stick to the Pilates exercise program for the entire trial.
Exclusion criteria were applied to patients with preexisting injuries or conditions that could affect Pilates exercise participation and those with contraindications or exacerbating conditions from such exercises.
Further criteria were currently participating in other intensive exercise or rehabilitation programs and inability to give informed consent due to cognitive or communicative issues
Study Type
Interventional
Enrollment (Estimated)
94
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: Hany M Elgohary, PhD
- Phone Number: 00201093182291
- Email: hmielgohary@gmail.com
Study Locations
-
-
Dakahlia
-
Mansoura, Dakahlia, Egypt, 57357
- Recruiting
- Faculty of physical therapy, Delta university for science and technology
-
Contact:
- Hany M Elgohary, PhD
- Phone Number: 00201093182291
- Email: hmielgohary@gmail.com
-
-
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
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Participants had to be between 18 and 45 years old,
- have had sports hernia for two to ten weeks
- be willing and able to attend and stick to the Pilates exercise program for the trial's entire duration
Exclusion Criteria:
- patients with preexisting injuries or conditions that could affect Pilates exercise participation
- those with contraindications or exacerbating conditions from such exercises.
- currently participating in other intensive exercise or rehabilitation programs
- inability to give informed consent due to cognitive or communicative issues.
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental
will receive a combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound.
|
The core and hip muscles will be targeted through a customized workout program consisting of exercises such as Breathing, Planks, Side- Planks, Weighted lunges, Glute Bridge, Clamshell, Half-Kneeling Hip Flexor Stretch, Swan dive, Roll down, Ab curls, and Shoulder bridge, Low-intensity Ultrasound , and low level laser therapy
|
|
Active Comparator: Control
will be given Low-level laser therapy and low-intensity ultrasound
|
The core and hip muscles will be targeted through a customized workout program consisting of exercises such as Breathing, Planks, Side- Planks, Weighted lunges, Glute Bridge, Clamshell, Half-Kneeling Hip Flexor Stretch, Swan dive, Roll down, Ab curls, and Shoulder bridge, Low-intensity Ultrasound , and low level laser therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale
Time Frame: 12 weeks
|
Typically, it consists of a 10 cm horizontal or vertical line with no pain at one end and the highest pain level at the other end.
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower Extremity Functional Scale
Time Frame: 12 weeks
|
Consists of 20 items that assess the ability to perform activities related to lower extremity function, such as standing, walking, stair climbing, and balance.
|
12 weeks
|
|
Harris Hip Score
Time Frame: 12 weeks
|
this tool is used to evaluate patients with hip conditions such as femoral neck fracture or OA.
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Estimated)
June 19, 2024
Primary Completion (Estimated)
September 20, 2024
Study Completion (Estimated)
September 30, 2024
Study Registration Dates
First Submitted
June 18, 2024
First Submitted That Met QC Criteria
June 18, 2024
First Posted (Actual)
June 24, 2024
Study Record Updates
Last Update Posted (Actual)
June 24, 2024
Last Update Submitted That Met QC Criteria
June 18, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- F.P.T 2307016
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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