- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07493083
Acute Effects of Posterior Talar Glide Mobilization
The Acute Effect of Posterior Talar Glide Mobilization on Weight Bearing Dorsiflexion Range of Motion and Walking Speed : A Randomized Sham-Controlled Trial
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tuğba GÖNEN, Asisst. Prof. Dr.
- Phone Number: 505 090 58 46
- Email: tugba.badat@hku.edu.tr
Study Locations
-
-
Şahinbey
-
Gaziantep, Şahinbey, Turkey (Türkiye), 27000
- Hasan Kalyoncu University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants aged between 18 and 45,
- Participants who have agreed to take part in the study on a voluntary basis,
- Participants with no history of lower limb surgery
Exclusion Criteria:
- Those with acute ankle pain or inflammation,
- Those with ankle instability,
- Those with a history of lower limb surgery within the last 6 months,
- Those with balance or vestibular disorders,
- Those with chronic conditions,
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mobilization Group
Movement Combined with Weight-Shifting Mobilisation: A non-elastic band is secured between the patient's distal leg and the therapist's waist. Mobilisation begins with the patient standing in a comfortable upright position. The therapist applies a continuous posteroanterior gliding force to the tibia via the band by shifting their weight backwards. This technique functionally mimics the posterior glide mechanism of the talus. The participant is asked to perform a slow dorsiflexion to the end of the range of motion. During this, the therapist maintains the posterior glide stimulus on the talus. Once the end point is reached, the glide force is maintained for 10 seconds. One set of 10 repetitions of mobilisation is performed. - Movement Combined with Mobilisation Without Weight-bearing The ankle is stabilised using a non-elastic band, and the therapist applies a posterior glide to the talus. During the posterior glide, the foot is supported by the forearm or leg. |
Movement Combined with Weight-Shifting Mobilisation The therapist applies a continuous posteroanterior gliding force to the tibia via the strap by shifting their weight backwards. This technique functionally mimics the posterior gliding mechanism of the talus. The patient is asked to perform a slow dorsiflexion to the end of their range of motion. During this, the therapist maintains the posterior gliding force on the talus. Once the end point is reached, the gliding force is maintained for 10 seconds. One set of 10 repetitions of mobilisation is performed. - Movement Combined with Mobilisation Without Weight Shifting The participant lies supine with the tibia in contact with the treatment table, whilst the foot and ankle are left free at the edge of the table. The ankle is stabilised with a non-elastic band, and the therapist applies posterior glide to the talus. |
|
Sham Comparator: Sham Group
Both mobilisation techniques and positions were explained to the participants; however, although the therapist positioned the ankle in the glide position, no sliding movement was performed, and the ankle was held in that position for 10 seconds. Posterior talar glide mobilisation and dorsiflexion measurements were performed on both the affected and unaffected ankles. All measurements will be repeated three times-once before and three times after treatment-and the average values will be recorded. |
Both mobilisation techniques and positions were explained to the participants; however, although the therapist assumed the glide position, no sliding movement was performed, and the participants were held in that position for 10 seconds. Posterior talar glide mobilisation and dorsiflexion measurements were performed on both the affected and unaffected ankles. All measurements will be repeated three times each-before and after treatment-and the average values will be recorded. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight Bearing Lunge Testi
Time Frame: through of the study, average 1 day
|
The WBLT is a valid and reliable clinical measurement method widely used to identify dorsiflexion restrictions, particularly in individuals with chronic ankle instability, and to monitor changes occurring during the rehabilitation process.
Its concurrent validity has been demonstrated in the literature using both angular and distance-based measurement methods.
During measurement, the maximum lunge distance between the big toe and the wall will be recorded in centimetres using a standard tape measure fixed to the floor.
Participants will undergo bilateral assessment during the test.
Participants will be asked to touch the wall with their knees without lifting their heels off the ground.
A vertical reference line on the floor will be used to minimise subtalar joint compensation and ensure measurement standardisation.
The contralateral limb will be positioned comfortably behind the tested limb, and participants will be permitted to place their hands on the wall for balance.
|
through of the study, average 1 day
|
|
10-meter walk test
Time Frame: through of the study, average 1 day
|
The test is a valid and reliable assessment method widely used in clinical and research settings to measure an individual's walking speed over a short distance.
The test will be conducted on a flat, non-slip surface.
The total walking distance will be set at 14 metres; the first 2 metres will be designated as an acceleration zone, the final 2 metres as a deceleration zone, and the middle 10-metre section as the measurement zone.
Participants will be asked to walk the specified distance at a natural walking speed that feels comfortable to them.
The measurement will be taken by recording the time elapsed from the moment the participant enters the central 10-metre section until the moment they exit it, using a stopwatch to record the time in seconds.
The test will be repeated three times, and the average of the measurements will be used in the analysis.
|
through of the study, average 1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tuğba GÖNEN, Asisst. Prof. Dr., Hasan Kalyoncu University
Publications and helpful links
General Publications
- Bennell KL, Talbot RC, Wajswelner H, Techovanich W, Kelly DH, Hall AJ. Intra-rater and inter-rater reliability of a weight-bearing lunge measure of ankle dorsiflexion. Aust J Physiother. 1998;44(3):175-180. doi: 10.1016/s0004-9514(14)60377-9.
- Chisholm MD, Birmingham TB, Brown J, Macdermid J, Chesworth BM. Reliability and validity of a weight-bearing measure of ankle dorsiflexion range of motion. Physiother Can. 2012 Fall;64(4):347-55. doi: 10.3138/ptc.2011-41.
- Hall EA, Docherty CL. Validity of clinical outcome measures to evaluate ankle range of motion during the weight-bearing lunge test. J Sci Med Sport. 2017 Jul;20(7):618-621. doi: 10.1016/j.jsams.2016.11.001. Epub 2016 Nov 23.
- Saito Y, Nakamura S, Tanaka A, Watanabe R, Narimatsu H, Chung UI. Evaluation of the validity and reliability of the 10-meter walk test using a smartphone application among Japanese older adults. Front Sports Act Living. 2022 Oct 4;4:904924. doi: 10.3389/fspor.2022.904924. eCollection 2022.
- Vicenzino B, Branjerdporn M, Teys P, Jordan K. Initial changes in posterior talar glide and dorsiflexion of the ankle after mobilization with movement in individuals with recurrent ankle sprain. J Orthop Sports Phys Ther. 2006 Jul;36(7):464-71. doi: 10.2519/jospt.2006.2265.
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2026/044
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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