Ultrasonographic Effects of Fascia Correction Kinesiotaping
Investigation of the Physiological Effects of Fascia Correction Kinesiotaping in Healthy Adults: An Ultrasonographic Study
1 other identifier
interventional
80
1 country
1
Brief Summary
Single-center, within-subject repeated-measures study The aim of the present study was to investigate the acute effects of kinesiotaping applied using the fascia correction technique with different tension levels on fascial layers and associated musculature in healthy individuals. Outcome measurements. The primary outcome was the ultrasonographically measured thickness of the fascial layers, while secondary outcomes included the thickness of the superficial and deep flexor muscle layers and the subcutaneous tissue.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable healthy
Started May 2024
Shorter than P25 for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2024
CompletedFirst Submitted
Initial submission to the registry
July 9, 2026
CompletedFirst Posted
Study publicly available on registry
July 15, 2026
CompletedJuly 15, 2026
July 1, 2026
4 months
July 9, 2026
July 9, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
The superficial antebrachial fascia thickness
ultrasonographic measurements were obtained from the dominant forearm at the mid-forearm level. the hyperechoic linear structure separating the subcutaneous tissue from the superficial flexor muscles was defined as superficial antebrachial fascia thickness
Baseline and 30 minutes after two different interventions (different tensions). A one-week washout period was implemented between applications
The deep antebrachial fascia thickness
Ultrasonographic measurements were obtained from the dominant forearm at the mid-forearm level. the hyperechoic linear structure separating the superficial and deep flxor muscles was defined as superficial antebrachial fascia thickness
Baseline and 30 minutes after two different interventions (different tensions). A one-week washout period was implemented between applications
Secondary Outcomes (3)
the subcutaneous tissue thickness
Baseline and 30 minutes after two different interventions (different tensions). A one-week washout period was implemented between applications
Forearm Superficial Flexor Muscle Thickness
Baseline and 30 minutes after two different interventions (different tensions). A one-week washout period was implemented between applications
Forearm deep flexor muscle thickness measured by B-mode ultrasonography (millimeters)
Baseline and 30 minutes after two different interventions (different tensions). A one-week washout period was implemented between applications
Study Arms (1)
Healthy Volunteers
EXPERIMENTALParticipants received kinesiotaping using the fascia correction technique at different tension levels according to the study protocol. Each participant underwent all intervention conditions, and ultrasonographic measurements were performed before and after each application.
Interventions
Eligibility Criteria
You may qualify if:
- A total of 80 healthy volunteers aged 18 years or older were included in the study. Participants had no current or previous serious musculoskeletal injury, pain, or neurological disorder affecting the upper extremity within the past six months
You may not qualify if:
- Individuals were excluded if they were pregnant; regularly participated in high-level athletic training or competitive sports, had a history of skin allergy to adhesive materials; or had previous kinesiotaping application within the last month.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Haydarpaşa Numune Training and Research Hospital
Istanbul, Turkey (Türkiye)
Study Officials
- STUDY CHAIR
Elem Yorulmaz, Prof
Haydarpasa Numune Training and Research Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Medical Doctor
Study Record Dates
First Submitted
July 9, 2026
First Posted
July 15, 2026
Study Start
May 1, 2024
Primary Completion
August 30, 2024
Study Completion
August 30, 2024
Last Updated
July 15, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share