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Effect of external ankle support in patients with chronic ankle instability

Effect of ankle support orthosis and kinesiotape on force control, muscle strength, and kinesiphobia in subjects with chronic ankle instability: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200315046784N3
Enrollment
60
Registered
2023-11-28
Start date
2023-12-11
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

chronic ankle instability. Other instability, ankle and foot

Interventions

Intervention 1: Intervention group: Group A will be received an ankle support orthosis. The patients will be asked to wear the orthosis for 4 weeks. Intervention 2: Intervention group: Group B: kinesi

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: aged 18 - 40. at least one significant ankle sprain at least 12 months ago that resulted in pain, swelling, and physical activity restriction for at least 1 day. have not sprained their ankle within the six weeks prior to study onset. feeling of instability, at least two episodes of giving way in the past 6 months. Ankle instability Instrument: answer "yes" to at least 5 yes/no questions (This should include question 1, plus 4 others) Cumberland Ankle Instability Tool. Score of =<24. 20 min or greater of moderate physical activity level at least 3 days. having no mechanical instability.

Exclusion criteria

Exclusion criteria: History of lower extremity injury, fracture, surgery or acute trauma in either lower extremity in the previous 3 months, or time since the last sprain of less than 3 months. diabetes, neuropathies, neurological pathology. consumption of muscle relaxant during research period. not receiving of ankle orthosis, kinesiotape, and physical therapy over the last 6 months. leg length discrepancies. rheumatoid arthritis. congenital deformities.

Design outcomes

Primary

MeasureTime frame
Force sense. Timepoint: before and after 4 weeks. Method of measurement: Isokinetic Dynamometer.;Force steadiness. Timepoint: before and after 4 weeks. Method of measurement: Isokinetic Dynamometer.

Secondary

MeasureTime frame
Evertor muscles strength eccentric and concentric contractions. Timepoint: before and after 4 weeks. Method of measurement: Isokinetic dynamometer.;Kinesiophobia/ fear of movement. Timepoint: before and after 4 weeks. Method of measurement: Tampa scale of kinesiphobia.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Azadinia

Iran University of Medical Sciences

azadinia.fatemeh@yahoo.com+98 21 2222 8051

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026