Management of Acute Lateral Ankle Sprains

NCT03527121 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 112

Last updated 2020-04-09

No results posted yet for this study

Summary

This study evaluates the effectiveness of pain guided early weight bearing as a means to enhance the outcome of acute lateral ankle sprain. Half of the participants will receive advice and instructions in pain guided early weight bearing plus a written home-based exercise program, while the other half will receive advice and instructions following standard operating procedures at site.

Conditions

  • Ankle Sprains

Interventions

OTHER

ESP physiotherapy

A single session with advice and instructions from an ESP physiotherapist in rest, ice, compression and elevation AND pain guided early weight bearing plus a written home-based exercise program.

OTHER

Usual care

A single session with advice and instructions from a physician in rest, ice, compression and elevation (usual care group).

Sponsors & Collaborators

  • University Hospital Bispebjerg and Frederiksberg

    collaborator OTHER
  • Regionshospitalet Horsens

    collaborator OTHER
  • University of Copenhagen

    collaborator OTHER
  • Slagelse Hospital

    collaborator OTHER
  • Christian Olsen

    lead OTHER

Principal Investigators

  • Christian P Olsen, PT, Msc · Department of Physiotherapy and Occupational Therapy, Slagelse Hospitals.

  • Marius Henriksen, PT, Prof. · University of Copenhagen and Bispebjerg-Frederiksberg Hospital

  • Søren T Skou, PT, PhD · University of Southern Denmark and Naestved-Slagelse-Ringsted Hospitals.

  • Mikael Elsborg, PT · The Regional Hospital in Horsens

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-22
Primary Completion
2019-12-15
Completion
2020-12-15

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03527121 on ClinicalTrials.gov