Actively Recruiting

Age: 18Years +
All Genders
ID07054892

Assessment of the Quality of Life of Patients Visiting the Emergency Department Following an Ankle Sprain Considering Severity Grade and Follow-Up Care

Led by Centre Hospitalier de Saint-Brieuc · Updated on 2025-07-11

176

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the recovery of quality of life in adults who visit the emergency department for an ankle sprain. The study focuses on assessing how well participants regain their baseline quality of life three months after the injury. It also considers the severity of the sprain and the type of follow-up care received, such as visits to physicians or physiotherapists. Participants will complete the FAAM-ADL questionnaire, a self-assessment tool measuring foot and ankle functional ability, first when they arrive at the emergency department. A second assessment using the same questionnaire will be done three months later by email or phone. The severity of the ankle sprain will be determined by the physician’s clinical evaluation at the initial visit. During the study, researchers will compare participants’ functional ability and quality of life before and three months after the injury. This comparison will help evaluate recovery progress. The study is observational, and participants will be monitored without receiving experimental treatments. The total participation involves the initial emergency visit and a follow-up assessment three months later.

CONDITIONS

Brief Title

Assessment of the Quality of Life of Patients Visiting the Emergency Department of the Saint-Brieuc Hospital Following an Ankle Sprain

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Recent ankle trauma
  • Initial consultation at the emergency department of Saint-Brieuc
Not Eligible

You will not qualify if you...

  • Surgical treatment following the trauma
  • Fracture resulting from the trauma
  • Ligament or bone injury to either lower limb within 6 months prior to the trauma
  • Injury to another joint during the trauma causing functional impairment
  • Adult under legal protection or deprived of liberty
  • Pregnant woman

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) at the emergency department

Monitoring

Duration - 3 months

Participants complete self-assessments of their ankle function and quality of life to evaluate recovery after the sprain.

1 follow-up assessment by email or phone at 3 months

Trial Site Locations

Total: 1 location

1

Centre Hospitalier de Saint-Brieuc - Paimpol - Tréguier

Saint-Brieuc, France, 22000

Actively Recruiting

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Research Team

A

Alexandre CAILLAUD

S

Sylvain GEFFROY

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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