Shin SplintNCT05931510
Release Versus Post Isometric Relaxation Among Futsal Players With Shin Splints
A study testing Myofscual release and Post isometric relaxation. in people with Shin Splint, run by Riphah International University at 1 site in Pakistan.
Trial summary
The aim of the study is to determine the effects of myofascial release versus post isometric relaxation among futsal players with shin splints Read more about this study
- Who is it for?
- Ages 20 to 30 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Shin Splint
- What is being tested?
- Myofscual release and Post isometric relaxation.
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 32 participants
- Where
- 1 sitePakistan
- Study dates
- 22 Nov 2022to 25 Jul 2023
- 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 20 to 30 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Subjects have leg pain with exertion of more than 1 or 2 hours
- Participants age 20-30 years
- Participants have MTSS for more than 2 weeks
- Subjects have No previous history of trauma to legs
- Subject having Local pain on lower anterior leg Gradual cessation of the offending activity
Who cannot join
- • Subjects have medical history of systemic disease
- Subjects have Medical history of cardiovascular disease
- Participants with History of metastatic diseases
- Any trauma or pathology of lower limb Participants having Neuropathy of lower extremity
Trial locations and contacts
1 site in 1 country.
Pakistan1 site, 1 recruiting
- Recruiting
Model town hospital
Lahore, Punjab Province
About this study
Official title: Effects of Myofascial Release Versus Post Isometric Relaxation Among Futsal Players With Shin Splints
The aim of the study is to determine the effects of myofascial release versus post isometric relaxation among futsal players with shin splints
Read the detailed description
Previous literature did not compare the combined effects of both myofascial release and post isometric relaxation technique inn sgin splints patients so the purpose of this study is self-explanatory, with the basic goal of comparing these two techniques to determine their effects on patient Pain, and Functional disability thus improving overall performance of the futsal players.This study will be helpful in proposing proper treatment for shin splint, to make people aware of the condition rehabilitation and improving performance of the futsal players undergoing the condition. Thus it will be useful for the betterment of the players overall health and wellbeing.
- Conditions
- Shin Splint
- Being tested
- Myofscual release, Post isometric relaxation.
- Keywords
- Shin splint, Myofascial release, Post isometric relaxation
- Medical subject headings
- Medial Tibial Stress Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Myofscual releaseOther
Also called Hot pack
I will apply myofascial release on group A patients and observse its effects on shin splint
Post isometric relaxation.Other
Also called Hot pack
I will apply post isonetric relaxation on group b patients and observe effects on shin splint
| Study group | Role | What they receive |
|---|---|---|
| Group A | Experimental | Myofascial release Receives: Other: Myofscual release |
| Group B | Experimental | Post isometric relaxation Receives: Other: Post isometric relaxation. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Numeric pain rating scale
Numeric pain rating scale NPRS is a subjective measure in which Pain intensity is frequently measured on an 11-point pain intensity scale (PI-NRS), where 0=no pain and 10=worst possible pain.
Measured: 3 months
Lower extremity functional scale
Lower extremity functional scale LEFS is a valid, reliable, and responsive tool that can be used to measure function in patients with lower extremity musculoskeletal dysfunction
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jul 2023
- Study start22 Nov 2022
- Primary completion15 Jul 2023 (estimated)
- Study completion25 Jul 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Shin SplintStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 32 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Nosheen Manzoor, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05931510
- Sponsor's protocol ID
- REC/RCR & AHS/23/0425
- Status last verified
- Jun 2023
- First submitted
- 26 Jun 2023
- Last updated
- 5 Jul 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Myofascial Release Versus Post Isometric Relaxation Among Futsal Players With Shin Splints
- ClinicalTrials.gov ID
- NCT05931510
- Acronym / sponsor ID
- REC/RCR & AHS/23/0425
- Conditions
- Shin Splint
- Keywords
- Shin splint, Myofascial release, Post isometric relaxation
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 32 participants (estimated)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 22 Nov 2022 (actual)
- Primary completion
- 15 Jul 2023 (estimated)
- Study completion
- 25 Jul 2023 (estimated)
- First posted
- 5 Jul 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the study is to determine the effects of myofascial release versus post isometric relaxation among futsal players with shin splints
Detailed description
Previous literature did not compare the combined effects of both myofascial release and post isometric relaxation technique inn sgin splints patients so the purpose of this study is self-explanatory, with the basic goal of comparing these two techniques to determine their effects on patient Pain, and Functional disability thus improving overall performance of the futsal players.This study will be helpful in proposing proper treatment for shin splint, to make people aware of the condition rehabilitation and improving performance of the futsal players undergoing the condition. Thus it will be useful for the betterment of the players overall health and wellbeing.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group A | Experimental | Other: Myofscual releaseMyofascial release |
| Group B | Experimental | Other: Post isometric relaxation.Post isometric relaxation |
Who may qualify
- Ages
- 20 to 30 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- Subjects have leg pain with exertion of more than 1 or 2 hours
- Participants age 20-30 years
- Participants have MTSS for more than 2 weeks
- Subjects have No previous history of trauma to legs
- Subject having Local pain on lower anterior leg Gradual cessation of the offending activity
Key exclusion criteria (4 listed)
- • Subjects have medical history of systemic disease
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Myofscual releaseAlso: Hot packI will apply myofascial release on group A patients and observse its effects on shin splint | Other | Group A |
| Post isometric relaxation.Also: Hot packI will apply post isonetric relaxation on group b patients and observe effects on shin splint | Other | Group B |
Primary outcome
Numeric pain rating scale
Time frame: 3 months
Numeric pain rating scale NPRS is a subjective measure in which Pain intensity is frequently measured on an 11-point pain intensity scale (PI-NRS), where 0=no pain and 10=worst possible pain.
Lower extremity functional scale
Time frame: 3 months
Lower extremity functional scale LEFS is a valid, reliable, and responsive tool that can be used to measure function in patients with lower extremity musculoskeletal dysfunction
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Jul 2023.
- Individual participant dataSharing planned: No
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nosheen Manzoor principal investigator
Riphah International University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Myofscual release and Post isometric relaxation. in people with Shin Splint, run by Riphah International University at 1 site in Pakistan.
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 5 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 5 Jul 2023. 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 Pakistan. 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 Nosheen Manzoor (03236877879, nosheen.manzoor@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Numeric pain rating scale (time frame: 3 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 5 Jul 2023.