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Pilates ExercisesPESHRNCT06471725

Effectiveness of Adding Pilates Exercises to Sports Hernia Rehabilitation:a Comparative Clinical Trial

A study testing combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound in people with Pilates Exercises and Sports Hernia, run by Cairo University at 1 site in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 to 45 years, men only
Conditions the study is for
Pilates Exercises, Sports Hernia
What is being tested?
combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound
Could I receive a placebo?
No, everyone receives an active treatment
How many people
94 participants
Where
1 siteEgypt
Study dates
19 Jun 2024to 30 Sep 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Men only
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Hany M Elgohary, PhD contact

00201093182291

hmielgohary@gmail.com

Egypt1 site, 1 recruiting
  • Faculty of physical therapy, Delta university for science and technology

    Al Mansurah, Dakahlia Governorate, 57357

    Hany M Elgohary, PhD, 00201093182291, hmielgohary@gmail.com

    Recruiting

Other trials in Egypt

About this study

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

Read the 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

Being tested
combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasoundOther

    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

Study groups in NCT06471725
Study groupRoleWhat they receive
ExperimentalExperimentalwill receive a combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound.
Receives: Other: combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound
ControlActive comparatorwill be given Low-level laser therapy and low-intensity ultrasound
Receives: Other: combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual Analogue Scale

    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.

    Measured: 12 weeks

Secondary outcomes (2)
  1. Lower Extremity Functional Scale

    Consists of 20 items that assess the ability to perform activities related to lower extremity function, such as standing, walking, stair climbing, and balance.

    Measured: 12 weeks

  2. Harris Hip Score

    this tool is used to evaluate patients with hip conditions such as femoral neck fracture or OA.

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2024
  2. Study start19 Jun 2024 (estimated)
  3. Primary completion20 Sep 2024 (estimated)
  4. Study completion30 Sep 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
2X2 model
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
94 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06471725
Sponsor's protocol ID
F.P.T 2307016
Acronym
PESHR
Status last verified
Jun 2024
First submitted
18 Jun 2024
Last updated
24 Jun 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Elabd OM, Etoom M, Jahan AM, Elabd AM, Khedr AM, Elgohary HM. The Efficacy of Muscle Energy and Mulligan Mobilization Techniques for the Upper Extremities and Posture after Breast Cancer Surgery with Axillary Dissection: A Randomized Controlled Trial. J Clin Med. 2024 Feb 8;13(4):980. doi: 10.3390/jcm13040980.

    PubMed 38398293

Questions about this trial

What is this clinical trial studying?

A study testing combination of pilates exercises, Low-level laser therapy, and low-intensity ultrasound in people with Pilates Exercises and Sports Hernia, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 24 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Hany M Elgohary, PhD (00201093182291, hmielgohary@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual Analogue Scale (time frame: 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06471725, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2024; AzTrials last refreshed its copy on 8 Nov 2026.

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