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Balance and Proprioception Training Program in Patients With Chronic Ankle Sprains

The Effects of an Individualized Balance and Proprioception Training Program on Pain and Function in Patients With Chronic Ankle Sprains: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05920044
Enrollment
45
Registered
2023-06-27
Start date
2023-06-27
Completion date
2024-07-12
Last updated
2023-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankle Sprains

Brief summary

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

Interventions

OTHERbalance 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.

OTHERUsual care

Participants will continue their usual care, including general strength and flexibility exercises. No specific balance and proprioception training will be provided.

Sponsors

Ahram Canadian University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Changes in Pain intensityChanges in Pain intensity at baseline, 8 weeks, and 16 weeks follow upPain intensity will be measured using the Numeric Pain Rating Scale (NPRS)
Changes in Functional AbilityChanges in Functional ability at baseline, 8 weeks, and 16 weeks follow upFunctional ability will be assessed using the Foot and Ankle Ability Measure (FAAM)

Secondary

MeasureTime frameDescription
Changes in BalanceChanges in balance at baseline, 8 weeks, and 16 weeks follow upBalance will be assessed using the Star Excursion Balance Test (SEBT)
Changes in ProprioceptionChanges in proprioception at baseline, 8 weeks, and 16 weeks follow upProprioception will be measured using the joint position sense test with an ankle electrogoniometer
Incidence of Recurrent Ankle SprainsFrom post-intervention at 8 weeks to the end of the follow-up period at 16 weeksIncidence of recurrent ankle sprains during the follow-up period will be recorded

Countries

Egypt

Contacts

Primary ContactMohamed M ElMeligie, Ph.d
mohamed.elmeligie@acu.edu.eg+201064442032

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026