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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06395714
Other study ID # 2023-08-SBM_Composite
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 17, 2024
Est. completion date June 2027

Study information

Verified date May 2024
Source Clinique du Sport, Bordeaux Mérignac
Contact Guillaume Cordier, MD
Phone +33556181724
Email docteurcordier@yahoo.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ankle sprain is one of the most common pathologies in the general population (between 2.1 and 3.2 per 1000 patients per year). Nearly 40% of patients will develop chronic instability in the year following the sprain. We also know that a premature return to sport is a risk factor for developing chronic instability. However, despite the consensus of experts on the subject which have shown the key physiological elements to evaluate before resuming sport, no test or cohort of tests are proposed to allow a safe return to sport by reducing the risks of relapse. Some very recent studies have appeared on non-operated subjects but this remains a subject that is still too little studied, where the lack of consensus and objective criteria increases the risk of instability. Surgical treatment remains an effective option to reduce the risk of recurrence but failure of the latter can occur in approximately 13-37% of patients depending on the population, due to a relapse or a return to sport which does not correspond to expectations. of the patient. The objective of the study is therefore to evaluate the predictive nature of a composite test (ANKLE-GO) regarding the return to sport at the same level and the risks of recurrence.


Recruitment information / eligibility

Status Recruiting
Enrollment 116
Est. completion date June 2027
Est. primary completion date June 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Patient with objective chronic ankle instability who has failed medical treatment and undergone lateral ankle ligament repair surgery - Patient practicing a sporting activity at least 2 times a week - Patient able to read, write and understand French - Patient affiliated to a social security scheme Exclusion Criteria: - Minor or over 50 years of age - Pregnant or breast-feeding patient - Patient under guardianship, deprived of liberty or under court protection - Refusal to participate in research - Patient unable to understand or give informed consent - Patient having undergone associated surgical procedures modifying the postoperative course - Patient having undergone revision surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Personnalized physiotherapy
Following completion of the ankle go test, patients in "experimental" group will receive specific instructions for continuing their rehabilitation, which will be passed on to the physiotherapist responsible for the rehabilitation.
Usual physiotherapy
Following completion of the ankle go test, patients in "active comparator" group will receive usual physiotherapy

Locations

Country Name City State
France Clinique du Sport Bordeaux Merignac Mérignac

Sponsors (1)

Lead Sponsor Collaborator
Clinique du Sport, Bordeaux Mérignac

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary 1-year post-surgery return to sport : Tegner questionnaire evaluation of sport practice level with Tegner questionnaire : Likert scale from 0 (professionnal disability) to 10 (professionnal sport) before surgery (anterior practice) and year 1
Secondary Sports level at 1 year post-surgery compared with previous level Questionnaire "yes/no" Year 1
Secondary Number of hours of sport per week Self administered questionnaire before surgery (anterior practice) and year 1
Secondary Ankle instability scale (FAAM questionnaire : Foot and Ankle Ability Measure) self-administered questionnaire to measure patients' functional progress. It comprises two subscales: a 21-item daily activity subscale, and an 8-item sports subscale. For each subscale, each item is rated on a Likert scale from 0 to 4. before surgery (anterior practice) and month 3
Secondary Pain: EVA analog scale EVA scale from 0 (no pain) to 10 (maximal possible pain) month 1, month 3, month 6, year 1
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