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Recruiting NCT06645262

First-degree Ankle Sprains

Observational Ankle Sprain 1St Degree

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cryotherapy.
Who it may be relevant to
Registry conditions: Ankle Sprain 1St Degree. Basic parameters: from 18 Weeks · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Bosnia and Herzegovina
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Grade I ankle sprains are common, especially among athletes, women, teenagers, and physically active individuals. While over a million cases are reported annually, this represents only half of the total occurrences. These injuries can lead to complications like chronic ankle instability or osteoarthritis. Treatment often involves conservative methods, including the PRICEMMS protocol (protection, rest, ice, compression, elevation, modalities, medication, and support), while surgery is reserved for severe cases. Therapeutic exercises and rehabilitation play a key role in recovery. The Bowen technique, effective for other musculoskeletal issues, has not yet been extensively studied for Grade I ankle sprains.

Interventions

  • Other Cryotherapy
    cryotherapy, therapeutic exercises, the use of braces, and the Bowen technique.

Primary outcome measures

  • Subjective assessment of pain intensity [Time frame: 3 weeks]

Eligibility criteria

Inclusion criteria

  • Individuals diagnosed with Grade I acute ankle sprain confirmed by a specialist physician in radiology,
  • Age of participants ≥ 18 years,
  • Individuals of both sexes

Exclusion criteria

  • Recurrent ankle injury,
  • Acute ankle sprains of Grade II and III,
  • Presence of other physical and/or mental health issues.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Bosnia and Herzegovina · 1 center
  • Rehabilitation Centre Život — Mostar

Identifiers

NCT: NCT06645262 · A2024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗