Effects of MET vs Mulligan MWM on Pain, Disability & Balance in Athletes With Ankle Sprain
Unknown statusNot applicableNCT05393310
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Ankle Sprains are the most common injury in Athletes and have a high rate of recurrence, pain, dynamic balance and disability is the leading cause of season break in athletes with chronic ankle sprain so as we see post isometric relaxation and Mulligan MWM are the useful techniques used to minimize pain, improve dynamic balance and to restrain athlete from disability due to chronic ankle sprain. This study will be a randomized clinical trial,non probability convenience sampling technique will be used to collect the data. The sample size of athletes will be taken in this study to find the effect of post isometric relaxation and mulligan mobilization with movement in athletes.
Study details
- Official title
- Effects of Post Isometric Relaxation Versus Mulligan Mobilization With Movement on Pain, Disability and Dynamic Balance in Athletes With Chronic Ankle Sprain
- Conditions
- Chronic Ankle Sprain
- Interventions
- Other: post isometric relaxation
- Other: MWM group
- Sponsor
- Riphah International University
- Start date
- 2021-10-25
- Primary completion
- 2022-12
- Sex
- Male
- Age range
- from 20 Years to 35 Years
- Results posted
- No results posted in this snapshot
- Countries
- Pakistan
- Total sites listed
- 2
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Diagnosed cases of chronic ankle sprain (grade I or II) (3-4 months) * Players have spent at least one year in sports Exclusion Criteria: * • Players undergone surgery or had an accident. * Any malignant or chronic disease * Players with the history of fracture in the same ankle
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05393310