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Clinical Trials/NCT05859256
NCT05859256
Completed
Not Applicable

Efficacy of a Flossing Protocol and Manual Therapy in the Clinical and Functional Improvement of Young Subjects With Recurrent Ankle Sprains. A Randomized Clinical Study.

Universidad Católica San Antonio de Murcia1 site in 1 country24 target enrollmentMay 6, 2023
ConditionsYoung People

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Young People
Sponsor
Universidad Católica San Antonio de Murcia
Enrollment
24
Locations
1
Primary Endpoint
Change from baseline ankle range of motion after treatment and at 4 weeks
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The most frequent lateral ankle sprain mechanism consists of talocrural plantarflexion added to a subtalar inversion. The anterior talofibular ligament, in plantar flexion, suffers maximum stress, being very sensitive to injury mechanisms with inversion of the foot, being the cause of up to 70% of sprains. The risk of injury recurrence must be taken into account. In sports practice, this percentage of recurrence is especially relevant.

Randomized clinical study. Participants will be randomized to a control or experimental group. The dependent variable will be the range of motion in ankle dorsiflexion. Secondary variables will be pressure pain threshold, and stability of the foot and ankle. Three evaluations will be carried out: before the start of the study (T0), after the intervention (T1) and after a 4-week follow-up period (T2). All evaluations will be performed by one evaluator, blinded to player assignment The intervention consists of the application of a treatment protocol based on an initial active warm-up consisting of 3 active exercises, walking for 1 minute performing slow and controlled movement of the ankle, raising the heels, 15 repetitions, dorsiflexion of the ankle in the standing position. gentleman, 15 reps. Subsequently, the floss band will be placed, performing again the 3 active warm-up exercises with the band on. After this, the passive manual techniques will be carried out for the remaining time, removing the flossing at the end of the latter, and actively mobilizing again.

Registry
clinicaltrials.gov
Start Date
May 6, 2023
End Date
July 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Universidad Católica San Antonio de Murcia
Responsible Party
Principal Investigator
Principal Investigator

Rubén Cuesta-Barriuso, PhD

Principal Investigator

Universidad Católica San Antonio de Murcia

Eligibility Criteria

Inclusion Criteria

  • Young people between 18 and 22 years old
  • Who have suffered a previous sprain
  • No chronic or degenerative musculoskeletal pathologies of the ankle or knee
  • That they do physical activity regularly.

Exclusion Criteria

  • Have suffered a sprain in the last 6 months
  • Being receiving another physiotherapy treatment at the time of the study
  • Not signing the informed consent document.

Outcomes

Primary Outcomes

Change from baseline ankle range of motion after treatment and at 4 weeks

Time Frame: Screening visit, within the first seven days after treatment and after four weeks follow-up

Using an analog goniometer, range of motion was measured. This instrument has shown excellent reliability. The joint range in plantar and dorsiflexion was measured. The unit of measurement is degrees (the higher the degree, the greater the mobility).

Secondary Outcomes

  • Change from baseline foot and ankle stability after treatment and at 4 weeks(Screening visit, within the first seven days after treatment and after four weeks follow-up)
  • Change from baseline pressure pain threshold treatment and at 4 weeks(Screening visit, within the first seven days after treatment and after four weeks follow-up)

Study Sites (1)

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