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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05920044
Other study ID # 012/Ank-01200021
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 27, 2023
Est. completion date July 12, 2024

Study information

Verified date June 2023
Source Ahram Canadian University
Contact Mohamed M ElMeligie, Ph.d
Phone +201064442032
Email mohamed.elmeligie@acu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To examine the effects of an individualized balance and proprioception training program on pain, function, and the risk of recurrent ankle sprains.


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date July 12, 2024
Est. primary completion date June 27, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Adults aged 18-55 years - History of at least two ankle sprains within the last 12 months - Presence of ankle instability symptoms, such as recurrent giving way or chronic pain Exclusion Criteria: - Acute ankle injury within the last six weeks - Lower extremity fracture within the last six months - Other musculoskeletal or neurological disorders affecting the lower extremity - Inability to comply with study requirements

Study Design


Related Conditions & MeSH terms


Intervention

Other:
balance and proprioception training program.
The program will include exercises focused on improving ankle stability and joint position sense, such as single-leg stance, wobble board, and resistance band exercises. Participants will attend two supervised sessions per week and perform home-based exercises 3-4 times per week. Progression of exercises will be individualized based on participant performance and tolerance.
Usual care
Participants will continue their usual care, including general strength and flexibility exercises. No specific balance and proprioception training will be provided.

Locations

Country Name City State
Egypt Outpatient clinic of faculty of physical therapy, Ahram Canadian University Al ?ayy Ath Thamin Giza

Sponsors (1)

Lead Sponsor Collaborator
Ahram Canadian University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Pain intensity Pain intensity will be measured using the Numeric Pain Rating Scale (NPRS) Changes in Pain intensity at baseline, 8 weeks, and 16 weeks follow up
Primary Changes in Functional Ability Functional ability will be assessed using the Foot and Ankle Ability Measure (FAAM) Changes in Functional ability at baseline, 8 weeks, and 16 weeks follow up
Secondary Changes in Balance Balance will be assessed using the Star Excursion Balance Test (SEBT) Changes in balance at baseline, 8 weeks, and 16 weeks follow up
Secondary Changes in Proprioception Proprioception will be measured using the joint position sense test with an ankle electrogoniometer Changes in proprioception at baseline, 8 weeks, and 16 weeks follow up
Secondary Incidence of Recurrent Ankle Sprains Incidence of recurrent ankle sprains during the follow-up period will be recorded From post-intervention at 8 weeks to the end of the follow-up period at 16 weeks
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