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Comparison of Passive and Active Joint Mobilization for Chronic Ankle Instability

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ClinicalTrials.gov Identifier: NCT04630899
Recruitment Status : Not yet recruiting
First Posted : November 16, 2020
Last Update Posted : November 16, 2020
Sponsor:
Information provided by (Responsible Party):
Hyun-Joong Kim, Sahmyook University

Brief Summary:
The features of CAI were confirmed through studies that 64% to 77% had extra-articular conditions mainly related to calf tendon disorder. In addition, joints are laxity, sensory motors are deficient, and the range of dorsi flexion is decreased. this study is to investigate the effects of active joint mobilization(AJM) under weight-bearing conditions to stimulate various proprioceptors for CAI with deficiency in sensorimotor and postural control.

Condition or disease Intervention/treatment Phase
Musculoskeletal Manipulations Chronic Instability of Joint Ankle Joint Other: Active joint mobilization Other: Passive joint mobilization Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Comparison of Passive and Active Joint Mobilization for Chronic Ankle Instability: A Randomized Controlled Trial
Estimated Study Start Date : November 28, 2020
Estimated Primary Completion Date : December 20, 2020
Estimated Study Completion Date : January 31, 2021

Arm Intervention/treatment
Experimental: Active Joint Mobilization Other: Active joint mobilization
The participants bend his knees in a prone position. The physical therapist holds the medial malleolus with one hand and the lateral malleolus with the other. At the same time, the physical therapist touches the participant's soles to the sternum area and presses them in the dorsal direction. At this time, medial malleolus glides anterior and lateral malleolus glides posterior. The first procedure is to passively recognize movement. The second procedure is accompanied by active movement of the participant.

Experimental: Passive Joint Mobilization Other: Passive joint mobilization
PJM uses Maitland's Mobilization method, grade III (high amplitude in the end range of the joint and 1 second vibration in the middle range through linear motion in which tissue resistance is felt). The participant is in a supine position, and the physical therapist holds the talus with one hand and the tibia with the other hand, and performs joint mobilization in the posterior direction with the hand holding the talus.




Primary Outcome Measures :
  1. Ankle instability [ Time Frame: 4 weeks ]
    Consists of 9 questions, 3 to 0 points for 5 questions, 4 to 0 points for 2 questions, 5 to 0 points for 1 question, and 2 to 0 points for another question. A total score of 30 points is the highest, 28 points or more are stable ankle joints, and 24 points or less are unstable ankle joints. The higher the score, the closer to normal, and the lower the score, the lower the stability.

  2. Range of motion [ Time Frame: 4 weeks ]
    Measured based on the accelerometer sensor built into the mobile phone with a clinometer app. After fixing the mobile phone on the participant's sole, press "0 clear" to calibrate it to the initial value. The physical therapist asks the participant to "flex the foot in the dorsal direction " Measure a total of 2 times and record it as an average value.



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Ages Eligible for Study:   19 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • First ankle sprain one year before clinical trial
  • A score of less than 24 on the Cumberland Ankle Instability Tool (CAIT)
  • No ankle sprains occurred within 4 weeks of starting the test
  • Two or more more ankle sprains in the past month

Exclusion Criteria:

  • If you have a history of lower extremity surgery
  • In case of receiving treatment for the affected ankle within 1 month
  • If you have a psychological problem

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04630899


Contacts
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Contact: Hyun-Joong Kim, M.S. +82-10-8005-1460 doong18324@gmail.com

Sponsors and Collaborators
Sahmyook University
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Responsible Party: Hyun-Joong Kim, Principal Investigator, Sahmyook University
ClinicalTrials.gov Identifier: NCT04630899    
Other Study ID Numbers: 2020-3096-001
First Posted: November 16, 2020    Key Record Dates
Last Update Posted: November 16, 2020
Last Verified: November 2020

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Joint Instability
Joint Diseases
Musculoskeletal Diseases