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

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

Study Locations

    • Dakahlia
      • Mansoura, Dakahlia, Egypt, 57357
        • Recruiting
        • Faculty of physical therapy, Delta university for science and technology
        • Contact:

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.

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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