- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06392880
Comparison of Floss Band Application and Mulligan Mobilization
April 29, 2024 updated by: Emel Taşvuran Horata, Afyonkarahisar Health Sciences University
Comparison of the Effects of Floss Taping and Mulligan Mobilization on Ankle Joint Movement, Vertical Jump, Gait and Balance in Healthy Young Adults
This study will investigate the effects of Floss band application and Mulligan mobilization on ankle range of motion, vertical jump, gait and balance in active healthy young adults.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The effects of floss band application and mulligan mobilization on ankle range of motion, vertical jump, gait, and balance in active healthy young adults are unclear or limited due to a lack of studies.
There are also no other studies comparing the two interventions in healthy young adults.
Therefore, this study will investigate the effects of Floss band application and Mulligan mobilization on ankle range of motion, vertical jump, gait, and balance in active healthy young adults.
Study Type
Interventional
Enrollment (Estimated)
21
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
- Name: EMEL TAŞVURAN HORATA, PhD
- Phone Number: 05547759663
- Email: ethorata@gmail.com
Study Locations
-
-
-
Afyonkarahisar, Turkey, 03030
- Recruiting
- Afyonkarahisar Health Science University
-
Contact:
- EMEL TAŞVURAN HORATA, PhD
- Phone Number: 05547759663
- Email: ethorata@gmail.com
-
Contact:
- Email: ethorata@gmail.com
-
Principal Investigator:
- EMEL TAŞVURAN HORATA, PhD
-
Sub-Investigator:
- ERDAL HORATA, PhD
-
Sub-Investigator:
- ARİFE NUR KANYILMAZ
-
Sub-Investigator:
- HALİL İBRAHİM SOLAK, PhD
-
-
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:
- Being between the ages of 18-24 years,
- Not having any known disease
- Being recreationally active
- Body mass index between 18.5 and 29.9 kg/m2
Exclusion Criteria:
- Presence of cardiovascular, rheumatic, dermatologic, orthopedic or neurologic diseases
- History of injury or trauma in the last 6 months
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Floss Band
A floss band will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
|
A floss band will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
Mulligan mobilization will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
Participants will practice various weight-bearing active ankle motions simultaneously.
|
|
Experimental: Mulligan mobilization
Mulligan mobilization will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
|
A floss band will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
Mulligan mobilization will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
Participants will practice various weight-bearing active ankle motions simultaneously.
|
|
Other: Control
Participants will practice various weight-bearing active ankle motions.
|
A floss band will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
Mulligan mobilization will be applied to the ankle joint and the participant will practice various weight-bearing active ankle motions simultaneously.
Participants will practice various weight-bearing active ankle motions simultaneously.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Passive ankle joint range of motion
Time Frame: The assessment will be conducted before and immediately after the interventions.
|
Passive ankle range of motion will be evaluated by taking photographs.
Measurements will be made with Image-J program on the photograph.
|
The assessment will be conducted before and immediately after the interventions.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: EMEL TAŞVURAN HORATA, PhD, Afyonkarahisar Health Sciences University
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 (Actual)
February 14, 2024
Primary Completion (Estimated)
May 14, 2024
Study Completion (Estimated)
June 14, 2024
Study Registration Dates
First Submitted
April 26, 2024
First Submitted That Met QC Criteria
April 29, 2024
First Posted (Actual)
May 1, 2024
Study Record Updates
Last Update Posted (Actual)
May 1, 2024
Last Update Submitted That Met QC Criteria
April 29, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2024/02
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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