NCT07703943

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P75+ for not_applicable healthy

Timeline
Completed

Started May 2024

Shorter than P25 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2024

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

July 9, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 15, 2026

Completed
Last Updated

July 15, 2026

Status Verified

July 1, 2026

Enrollment Period

4 months

First QC Date

July 9, 2026

Last Update Submit

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

EXPERIMENTAL

Participants 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.

Other: Kinesiotaping

Interventions

Fascia correction technique kinesiotaping

Healthy Volunteers

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

Study Officials

  • Elem Yorulmaz, Prof

    Haydarpasa Numune Training and Research Hospital

    STUDY CHAIR

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

Locations