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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07449078
Enrollment
40
Registered
2026-03-04
Start date
2026-01-06
Completion date
2026-12-01
Last updated
2026-03-04

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

Conditions

Chronic Ankle Sprain, Chronic Ankle Sprains

Keywords

Chronic Ankle Sprain, CAS, CFT, Cognitive Functional Therapy, Behavior, Beliefs

Brief 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).

Detailed description

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). This study will follow a structured clinical research protocol designed to evaluate the effects of Cognitive Functional Therapy (CFT) on individuals with chronic ankle sprain. This study is an experimental clinical intervention with a two-time-point measurement design. The Cognitive Functional Therapy (CFT) program will be applied to individuals with chronic ankle sprain, and its effects will be evaluated at baseline (before intervention) and after the 12-week intervention. The study will take place between January 2026 and June 2026. All participants will undergo an initial eligibility screening by an orthopedic specialist prior to enrollment. Following informed consent, eligible participants will attend a baseline assessment session, complete validated self-report questionnaires, and then begin a 12-week individualized CFT program consisting of seven sessions. Interventions will be delivered by a trained physiotherapist with clinical experience in musculoskeletal rehabilitation and certification in CFT principles. All data collection, including digital files and paper records, will be securely stored in encrypted systems accessible only to the research team. At the conclusion of the 12-week program, participants will fill the same questionnaires they filled at the beginning of the study as an outcome measurement. The outcome measurements are VAS, TSK-17, and FAAM questionnaires.

Interventions

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.

Sponsors

Yeditepe University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 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

Design outcomes

Primary

MeasureTime frameDescription
FAAM12 WeeksFoot and Ankle Ability Measure
TSK-1712 WeeksTampa Scale of Kinesiophobia
VAS12 WeeksVisual Analogue Scale

Countries

Turkey (Türkiye)

Contacts

CONTACTAbdullah Omar A PT, MSc
abdullah.alwakil@std.yeditepe.edu.tr0090 531 699 4226
CONTACTDr. Öğr. Üyesi Elif Tuğçe Çil Elif Tuğçe Çil
tugce.cill@gmail.com0090 554 481 10 92
PRINCIPAL_INVESTIGATORAbdullah Omar Alwakil, Bachelor

Yeditepe University

STUDY_CHAIRDr. Öğr. Üyesi Elif Tuğçe Çil Çil, Dr. Ogr. Uyesi

Yeditepe University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026