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Recruiting Not applicable

Investigating the Effects of Cognitive Functional Therapy on Pain, Physical Function, and Kinesiophobia in Individuals With Chronic Ankle Sprain

NCT07449078 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-06
Last updated
2026-03-04

Condition(s) studied

Chronic Ankle SprainChronic Ankle Sprains

Investigational drug(s) / intervention(s)

Cognitive Functional Therapy

Cognitive Functional Therapy: Cognitive Functional Therapy is an integrated behavioral approach for individualizing the management of people with chronic pain, originally developed for Low Back Pain Patients. It uses a multidimensional "clinical reasoning framework" to identify key modifiable targets for management on the basis of careful listening to the individual's story and examining the individual's behavioral responses to pain. This approach enables the treating clinician to take individuals on a journey to effectively self-manage their chronic pain with a program that is tailored to their unique clinical presentation and context.

Study summary

The aim of this study is to investigate the effects of Cognitive Functional Therapy (CFT) on pain, physical function, and kinesiophobia in individuals with chronic ankle sprain (CAS).

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Ongoing pain or swelling, "giving way" episodes, and re-injury during sports or daily activity * Adults aged 18-65 years * History of lateral ankle sprain with symptoms persisting for more than 3 months * Continuing symptoms such as pain, instability, or activity limitations * Ability to understand and communicate in English or Arabic Exclusion Criteria: * History of ankle surgery within the past 12 months * Advanced ankle osteoarthritis or systemic inflammatory, neurological, or vestibular conditions * Currently undergoing physiotherapy for the same condition * Cognitive impairment or severe psychological disorder that could interfere with participation * Pregnancy or planned pregnancy during the study period * Any other condition deemed unsuitable by the research team

Primary outcome measure(s)

  • FAAM — 12 Weeks
    Foot and Ankle Ability Measure
  • TSK-17 — 12 Weeks
    Tampa Scale of Kinesiophobia
  • VAS — 12 Weeks
    Visual Analogue Scale

Trial sites (1)

FacilityCityRegionStatus
Yeditepe University Istanbul Ataşehir Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07449078 on ClinicalTrials.gov ↗ ← All trials in Turkey