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Effects of Hip Strength Training and Neuromuscular Electrical Stimulation on Functional Ankle Instability

T

Tianjin University of Sport

Status

Completed

Conditions

Ankle Injuries and Disorders

Treatments

Procedure: Neuromuscular electrical stimulation
Procedure: Hip strength training
Procedure: Conventional ankle training

Study type

Interventional

Funder types

Other

Identifiers

NCT06125158
TianjinSport

Details and patient eligibility

About

The goal of this clinical trial is to compare the effects of two methods of elevating hip muscle strength on functional ankle instability(FAI). . The main question[s] it aims to answer are:

  • Whether hip strength training and neuromuscular electrical stimulation of the gluteal muscles, respectively, based on conventional ankle training improves dysfunction in patients with FAI?
  • Is there a difference in the efficacy of the above two interventions for FAI?

Full description

Participants will be randomly divided into 3 groups (Experimental Group A, Experimental Group B and Control Group) to receive the intervention for 6 weeks. The Control Group will undergo conventional ankle interventions such as peri-ankle muscle strength training and ankle balance training; Experimental Group A will undergo hip muscle strength training based on the conventional training; and Experimental Group B will perform neuromuscular electrical stimulation of hip abductors and hip extensors based on the conventional training. Researchers will compare the three groups to see changes in hip muscle strength, lower extremity muscle activation, ankle muscle strength, proprioception, dynamic and static balance, and self-reported ankle function.

Enrollment

39 patients

Sex

All

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • History of at least one acute ankle sprain one year ago, accompanied by symptoms such as pain, swelling, and inability to participate in daily activities for more than one day.
  • Unilateral ankle sprains and or instability felt at least twice during the past year.
  • Last ankle sprain occurred greater than or equal to 1 month from the start of the experiment.
  • Cumberland Ankle Instability Tool (CAIT) score less than or equal to 27 points,
  • The results of Medial Talar Tilt Test and Anterior Draw Test are negative.
  • Body Mass Index (BMI)ranges from 18 to 25.

Exclusion criteria

  • History of lower extremity surgery or fracture.
  • History of brain injury or neurological disorders.
  • Acute injury to musculoskeletal structures of other joints of the lower extremities within 1 month, affecting joint integrity and function.
  • Participated in lower extremity rehabilitation or systematic athletic training after injury.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

39 participants in 3 patient groups

Control group
Active Comparator group
Description:
Participants in this group will receive conventional ankle interventions including ankle strength training and balance training. All treatments target the affected lower extremity for 40 minutes per session, once per day, 3 days per week for 6 weeks.
Treatment:
Procedure: Conventional ankle training
Experimental Group A
Experimental group
Description:
Participants in this group will be asked to perform conventional ankle training and hip strength training. The conventional ankle training routine for this group will have the same movements as the control group, but the volume of training will be half that of the control group, and the duration of training will be 20 min/session. Hip strength training will consist of elastic band resistance exercises, forward step-up and lateral step-up for 20 min/session. All treatments target the affected lower extremity for 40 minutes per session, once per day, 3 days per week for 6 weeks.
Treatment:
Procedure: Hip strength training
Procedure: Conventional ankle training
Experimental Group B
Experimental group
Description:
Participants in this group will be asked to perform conventional ankle training and neuromuscular electrical stimulation. The conventional ankle training routine for this group will have the same movements as the control group, but the volume of training will be half that of the control group, and the duration of training will be 20 min/session. Neuromuscular electrical stimulation aims to stimulate the gluteus maximus and gluteus mediums muscles of the affected lower limb. The researcher chose the "Neuromuscular Electrical Stimulation 1" mode for the treatment prescription (this prescription can output a variety of waveforms with frequencies varying continuously from 1 to 100 Hz to stimulate the target muscles alternately, effectively preventing muscle fatigue caused by a single stimulation) and set the stimulation time to 20 min per session. All treatments target the affected lower extremity for 40 minutes per session, once per day, 3 days per week for 6 weeks.
Treatment:
Procedure: Neuromuscular electrical stimulation
Procedure: Conventional ankle training

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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