Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
All Genders
NCT06552533

Comparison of Resistance Training With and Without Plyometric Exercises on Athletes With Chronic Ankle Instability.

Led by Riphah International University · Updated on 2024-08-14

24

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic ankle instability is characterized by a patient's being more than 12 months removed from the initial LAS and exhibiting a propensity for recurrent ankle sprains, frequent episodes or perceptions of the ankle giving way, and persistent symptoms such as pain, swelling, limited motion, weakness, and diminished self-reported function. This study will Compare Resistance Training with and without Plyometric exercises on Athletes with Chronic Ankle instability and changes will be recorded using different methods and tools. Patients will be randomly allocated into two different groups. Group A will be treated with resistance training and Group B will be treated with resistance training along with plyometric exercises . Participants will complete clinician-oriented tests. Participants of both groups will be evaluated before and after the application of respective interventions at the end of 8th week. Data will be analysed.

CONDITIONS

Official Title

Comparison of Resistance Training With and Without Plyometric Exercises on Athletes With Chronic Ankle Instability.

Who Can Participate

Age: 18Years - 35Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • History of at least 1 significant ankle sprain with symptoms and at least 1 day off from physical activity
  • Multiple episodes of ankle "giving way" or recurrent sprain in past 6 months
  • Completed FAAM questionnaire with scores below thresholds on ADL and Sports subscales
  • If both ankles qualify, the more affected ankle is considered for the study
  • Aged between 18 and 35 years
Not Eligible

You will not qualify if you...

  • Acute lower extremity injury within 3 months before the study
  • Participation in formal rehabilitation within 3 months before the study
  • History of lower extremity surgery or fracture requiring alignment in the involved limb
  • Diagnosed neurological disorders such as multiple sclerosis, Parkinson disease, or head injury

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sehat Medical Complex, Pakistan sports board complex

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

M

Muhammad Atif Javed, PP-DPT

CONTACT

A

Anam Dalawar, DPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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