Effect of PNF Training as an Intervention for Functional Ankle Instability in College Student

March 14, 2024 updated by: Ma Shuzhen
The lower limb stability test was carried out by MicroSwing 6.0 gravity center moving trajectory tester made in Germany.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

The test steps and methods are as follows:

  1. Before the test, arrange the subjects to be familiar with the lower limb stability test system and test environment, and master the test method.
  2. The subject stands barefoot and one foot in the center of the center of gravity movement trajectory tester, with his hands placed on his sides naturally, and maintains his body balance for 30 seconds.
  3. Record data of the test system.
  4. The measurement was repeated three times with a time interval of 5min. Collect the test data of the center of gravity moving trajectory tester, including swing frequency, coordination coefficient and stability coefficient, and get the best results of the three tests. The smaller the oscillation frequency and coordination coefficient are within a certain range, the better the stability is. The greater the value of stability coefficient is within a certain range, the better the stability is.

Study Type

Interventional

Enrollment (Estimated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Unilateral functional ankle instability;
  2. Have not received formal rehabilitation treatment or informal rehabilitation treatment within the past month;
  3. Voluntarily accept the treatment in this study and ensure to complete the training tasks arranged by the therapist;
  4. Aged between 18 and 23 years old;

Exclusion Criteria:

  1. Does not meet the above diagnostic criteria;
  2. Ankle pain caused by infectious diseases;
  3. suffering from severe neurological diseases;
  4. Soft tissue damage near the ankle joint;
  5. Other joints outside the ankle are unstable.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: PNF training group
The experimental group will undergo 60 minutes of PNF training.
The subjects underwent rehabilitation training for 8 weeks, three times a week (Monday, Wednesday and Friday, 6:00 PM to 10:00 PM in the Physical Education College of Guangxi Normal University), and the rehabilitation training time was about 40-45 minutes per person. Before each rehabilitation training, the subjects warmed up the ankle and lower leg muscles for 5 minutes, followed by the corresponding rehabilitation training for 30-35 minutes, and relaxed the ankle and lower leg muscles for 5 minutes after the training.
Other: Control training group
The control group will follow the curriculum standards set by the Sports University.
The subjects underwent rehabilitation training for 8 weeks, three times a week (Monday, Wednesday and Friday, 6:00 PM to 10:00 PM in the Physical Education College of Guangxi Normal University), and the rehabilitation training time was about 40-45 minutes per person. Before each rehabilitation training, the subjects warmed up the ankle and lower leg muscles for 5 minutes, followed by the corresponding rehabilitation training for 30-35 minutes, and relaxed the ankle and lower leg muscles for 5 minutes after the training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
CAIT score
Time Frame: Baseline, post-test after 8 weeks

CAIT consists of 9 questions with a total of 30 points, scoring ≦27 points for diagnosis of functional ankle instability, 28 points and above for diagnosis of non-functional ankle instability.

  1. Before issuing the questionnaire, explain the contents of the questionnaire to the subjects in detail, and the subjects fill in the questionnaire truthfully according to their own situation.
  2. The CAIT score of the subjects was calculated and recorded.
  3. If you fill in the questionnaire incorrectly, you need to fill it again and keep a record
Baseline, post-test after 8 weeks
Lower limb stability test
Time Frame: Baseline, post-test after 8 weeks

The lower limb stability test was carried out by MicroSwing 6.0 gravity center moving trajectory tester made in Germany. The test steps and methods are as follows:

  1. Before the test, arrange the subjects to be familiar with the lower limb stability test system and test environment, and master the test method.
  2. The subject stands barefoot and one foot in the center of the center of gravity movement trajectory tester, with his hands placed on his sides naturally, and maintains his body balance for 30 seconds.
  3. Record data of the test system.
  4. The measurement was repeated three times with a time interval of 5min. Collect the test data of the center of gravity moving trajectory tester, including swing frequency, coordination coefficient and stability coefficient, and get the best results of the three tests.
Baseline, post-test after 8 weeks
Star offset balance test
Time Frame: Baseline, post-test after 8 weeks

The subjects stood in the center of the star chart with the affected side foot as the supporting foot, with bare feet and one foot in the center. The healthy side foot was extended forward, outward front, outer front, outer back, back, inner back, inner and inner front respectively to the farthest distance as far as possible. The supporting foot was extended in the counterclockwise direction when the left foot was used, and the supporting foot was extended in the clockwise direction when the right foot was used. The subject withdrew the non-supporting foot and resumed standing with both feet and rested for 5 seconds. The data of each extension of the subject was recorded, and the farthest score was measured three times. The furthest results in each direction were standardized with the subjects' lower limb length, and the data were recorded.

(4) The furthest scores in each direction were standardized with the subjects' lower limb length, and the data were recorded.

Baseline, post-test after 8 weeks
Muscle strength test
Time Frame: Baseline, post-test after 8 weeks

MicroFET2 hand-held muscle strength tester made in Germany was used for muscle strength test. The test steps and methods are as follows:

  1. Before the test, arrange the subjects to be familiar with the handheld muscle strength test system and test environment, and master the test method.
  2. The subject took off his shoes and socks and lay on his back on the recovery bed with his hands naturally placed on his chest. The muscle strength of the subject's dorsalis, plantar flexus, varus and valgus were tested respectively.
  3. Record data of the test system.
  4. The measurement was repeated 5 times in each direction of movement. The test data of handheld muscle strength tester were collected, including the muscle strength of ankle dorsiflexion, plantar flexion, varus and valgus, and the best results of 5 tests were obtained.
Baseline, post-test after 8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 30, 2024

Primary Completion (Estimated)

May 30, 2024

Study Completion (Estimated)

June 20, 2024

Study Registration Dates

First Submitted

March 5, 2024

First Submitted That Met QC Criteria

March 5, 2024

First Posted (Actual)

March 13, 2024

Study Record Updates

Last Update Posted (Actual)

March 15, 2024

Last Update Submitted That Met QC Criteria

March 14, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Shuzhen Ma

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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