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Chronic Ankle InstabilityNCT06682897

Simplified Tai Chi Exercises to Improve Function in People With Chronic Ankle Instability

A study testing Tai Chi training in people with Chronic Ankle Instability, run by Loughborough University at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this interventional trial is to evaluate the effectiveness of the simplified four-week Tai Chi training in improving function in people with chronic ankle instability. The main questions it aims to answer are: 1. Does the 4-week Tai Chi training improve ankle neuromuscular responses? 2. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Chronic Ankle Instability
What is being tested?
Tai Chi training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
36 participants
Where
1 siteUnited Kingdom
Study dates
5 Aug 2024to 2 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Aged from 18 to 40
  • A history of at least one significant lateral ankle sprain was associated with inflammatory symptoms (pain, swelling, etc) and disrupted activity
  • The initial sprain must have occurred at least 12 months prior to study enrolment
  • The most recent injury must have occurred more than 3 months prior to study enrolment
  • Reports of feeling instable or "giving way" during daily activities or physical activities and experienced at least 2 episodes in the 6 months prior to study enrolment
  • Scoring ≤25 on the Cumberland Ankle Instability Tool

Who cannot join

  • Any previous fractures or surgeries on the lower limbs
  • Have other muscle, joint or nerve disorders that affect the function of the lower limbs
  • Chest pain at rest, dizziness during rest, heart condition, or doctor's advice not to exercise without medical supervision
  • Currently enrolled in other ankle rehabilitation programmes
  • Already a Tai Chi practitioner
  • Pregnant
  • Allergic to adhesive tapes

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Loughborough University

    Loughborough, Leicester, LE113TU

Other trials in United Kingdom

About this study

The goal of this interventional trial is to evaluate the effectiveness of the simplified four-week Tai Chi training in improving function in people with chronic ankle instability. The main questions it aims to answer are:

  1. Does the 4-week Tai Chi training improve ankle neuromuscular responses?
  2. Does the 4-week Tai Chi training enhance ankle proprioception?
  3. Does the 4-week Tai Chi training improve ankle muscle strength?
  4. Does the 4-week Tai Chi training boost balance performance?
  5. Does the 4-week Tai Chi training enhance subjective ankle stability and quality of life?
Read more

Researchers will compare Tai Chi training to self-management to see if this Tai Chi training works to enhance ankle stability performance.

Participants will:

  1. Take self-management and Tai Chi training, and each for 4 weeks
  2. Visit the labs every 4 weeks for biomechanical measurements and questionnaires, totally 3 times.
Read the detailed description

Tai Chi is a traditional Chinese exercise practiced by millions worldwide to stay active and improve health. Based on muscle activation levels across the full set of movements (108 forms), we developed a simplified 16-form Tai Chi routine to enhance ankle stability for individuals with chronic ankle instability.

To evaluate the benefits of this simplified 16-form version for ankle function in people with chronic ankle instability, we are recruiting individuals managing symptoms of chronic ankle instability for a 4-week training program and assess their ankle-related function three times. All participants are randomly allocated to both the Tai Chi training group or a self-management control group, while maintaining their usual lifestyle and exercise routines throughout the study. All participants will complete the same training content and assessment tasks; participants in the control group will be offered the Tai Chi training following completion of the second outcome assessment.

The Tai Chi training includes a total of 12 sessions over 4 weeks, with three sessions per week, each lasting 1 hour (10 minutes of warm-up, 45 minutes of Tai Chi practice, and a 5-minute cool down). Each of the three functional assessments will include consistent measures, including muscle activation, proprioception, muscle strength, balance testing, and self-assessment scales (ankle function and quality of life).

Being tested
Tai Chi training
Keywords
ankle, Tai Chi

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Tai Chi trainingBehavioural

    60 minutes each session, three sessions per week, lasting 4 weeks for undertaking.

Study groups in NCT06682897
Study groupRoleWhat they receive
ExerciseExperimentalParticipants will be asked to choose three time slots per week to come to the lab, and each time slot will consist of a 1-hour workout that includes a 10-minute warm-up, a 45-minute Tai Chi practice, and a 5-minute cool-down.
Receives: Behavioral: Tai Chi training
ControlNo interventionParticipants replicated all the procedures of the exercise trial except for the different starting phase of the training.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Ankle neuromuscular reponses

    This includes two tasks, one is drop-landing, the other is ankle inversion perturbation. Each side will perform each task three times. Six electromyography muscle sensors will be placed on peroneus longus, peroneus brevis and tibialis anterior muscles to record muscle activity.

    Measured: From the date of randomization until the completion of three assessments. This evaluation will be conducted at 0, 4, and 8 weeks after enrollment, with a maximum duration of 8 weeks.

Secondary outcomes (4)
  1. Ankle proprioception

    Proprioception will be tested using both the Humac Norm dynamometer and the trapdoor devices.

    Humac: Participants' ankles will be moved to inversion positions of 10 and 20 degrees and eversion positions of 10 and 15 degrees under the Humac device. The degrees of their active and passive replication will be recorded.

    Trapdoor: The tilt angle will be adjusted using four wooden blocks to 10, 12, 14, and 16 degrees. Each angle will be repeated randomly 10 times, totaling 40 trials. The perceived height number for each trial will be recorded.

    Measured: From the date of randomization until the completion of three assessments. This evaluation will be conducted at 0, 4, and 8 weeks after enrollment, with a maximum duration of 8 weeks.

  2. Ankle muscle strength

    Ankle Muscle Strength will be assessed using the HUMAC Norm dynamometer. The assessment of eversion will be conducted at a speed of 30°/s (eccentric and concentric), and inversion will be conducted at a speed of 60°/s (eccentric and concentric). The peak of the participant's maximum effort three times will be recorded.

    Measured: From the date of randomization until the completion of three assessments. This evaluation will be conducted at 0, 4, and 8 weeks after enrollment, with a maximum duration of 8 weeks.

  3. Balance performance

    Static balance:

    Participants are asked to complete three trials of unipedal stance on both limbs in both open and close eyes. A total of 12 trials are required, with each trial lasting for 10 s.

    Dynamic balance:

    SEBT: Three times each side. The most distal aspect of the great toe on 0 (crossroad of eight lines) during the entire procedure.The maximum distance (centimeters) for each reach direction is recorded.

    DLBT: Three times each side. All participants start by moving their right leg clockwise and their left leg counterclockwise to each direction. After jumping to an outer target, participants need to return to the center target and stabilise for two seconds, then jump again to an outer target. The total time will be recorded.

    Measured: From the date of randomization until the completion of three assessments. This evaluation will be conducted at 0, 4, and 8 weeks after enrollment, with a maximum duration of 8 weeks.

  4. Questionnaire

    This includes the assessment of subjective ankle stability using the Cumberland Ankle Instability Tool and the Foot and Ankle Ability Measure questionnaire, as well as the evaluation of quality of life using the SF-12 questionnaire.

    Measured: From the date of randomization until the completion of three assessments. This evaluation will be conducted at 0, 4, and 8 weeks after enrollment, with a maximum duration of 8 weeks.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Nov 2024
  2. Study start5 Aug 2024
  3. Primary completion2 Dec 2024
  4. Study completion2 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
36 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06682897
Sponsor's protocol ID
17526
Status last verified
Jan 2026
First submitted
28 Oct 2024
Last updated
4 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data (IPD) will not be shared due to privacy concerns and institutional data protection policies.

Questions about this trial

What is this clinical trial studying?

A study testing Tai Chi training in people with Chronic Ankle Instability, run by Loughborough University at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Ankle neuromuscular reponses (time frame: From the date of randomization until the completion of three assessments. This evaluation will be conducted at 0, 4, and 8 weeks after enrollment, with a maximum duration of 8 weeks.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Feb 2026.

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