Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
NCT07190599

NMES With PNF for Ankle Sprain Rehabilitation

Led by Fooyin University · Updated on 2025-11-17

60

Participants Needed

1

Research Sites

43 weeks

Total Duration

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AI-Summary

What this Trial Is About

Ankle sprains are one of the most common sports injuries. In some people, they can lead to chronic ankle problems that affect daily life and sports performance. In this study, we want to see if combining neuromuscular electrical stimulation (NMES) with proprioceptive neuromuscular facilitation (PNF) can help improve these problems. We plan to recruit 60 participants, with 30 in the experimental group and 30 in the control group. The experimental group will receive PNF stretching with NMES, while the control group will only do PNF stretching. Both groups will have training three times a week for four weeks (12 sessions in total). We will test participants before and after the program, looking at pain, balance, range of motion, proprioception, strength, joint mobility, and functional limitations. We expect that 12 sessions will help improve chronic ankle problems, and that NMES combined with PNF will be more effective than PNF alone.

CONDITIONS

Official Title

NMES With PNF for Ankle Sprain Rehabilitation

Who Can Participate

Age: 18Years - 30Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-30 years
  • Adults with a history of ankle sprain
Not Eligible

You will not qualify if you...

  • Participants with ankle fractures
  • Participants with dislocations
  • Participants with grade III ankle sprains
  • Participants with bony restrictions
  • Participants with swelling
  • Participants with neuropathy
  • Participants with any other neuromuscular disorders

AI-Screening

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Trial Site Locations

Total: 1 location

1

Fooyin University

Kaohsiung City, No. 151, Jinxue Road, Daliao District, Taiwan

Actively Recruiting

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Research Team

I

I-Hsuan Chen

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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