Acute Effects of Upper Arm Tissue Flossing on Upper Extremity Performance and Power

NCT07670793 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2026-06-26

No results posted yet for this study

Summary

This randomized sham-controlled trial investigates the acute effects of upper arm tissue flossing on upper extremity performance and power in healthy adults. Tissue flossing is a compression-based intervention that involves wrapping an elastic band around a limb for a short period while performing movement exercises.

Twenty-eight healthy participants are randomly assigned to either an active tissue flossing group or a sham flossing group. The intervention is applied to the dominant upper arm. Upper extremity performance is assessed before the intervention and at 2 and 15 minutes after the intervention using the Closed Kinetic Chain Upper Extremity Stability Test (CKCUEST) and the Seated Medicine Ball Throw (SMBT).

The study aims to determine whether a single session of upper arm tissue flossing can produce immediate improvements in upper extremity stability, functional performance, and explosive power compared with a sham intervention

Conditions

  • Upper Extremity Performance
  • Healthy Volunteers
  • Tissue Flossing

Interventions

OTHER

Active Myofascial Compression

The floss band is applied to the participant's dominant upper arm by a licensed physiotherapist. Wrapping proceeds in a distal-to-proximal direction with approximately 50% overlap between layers, terminating just distal to the axilla. The band is stretched to a standardized elongation between 50% and 70% of its maximal length to generate moderate circumferential compression. Once wrapped, the participant performs a standardized 2-minute low-to-moderate intensity active movement sequence consisting of repeated elbow flexion/extension, shoulder flexion/extension, and forearm pronation/supination. The band is fully removed immediately following the 2-minute movement block

OTHER

Sham Myofascial Wrap

The floss band is applied to the participant's dominant upper arm by the same physiotherapist, maintaining identical therapist contact time, limb positioning, and overall session duration as the active group. However, the band is applied with less than 10% elongation, creating a loosely snug contact fit insufficient to generate meaningful circumferential compression or local vascular occlusion. Once wrapped, the participant performs the exact same 2-minute low-to-moderate intensity active movement sequence (elbow flexion/extension, shoulder flexion/extension, and forearm pronation/supination) before the band is fully removed.

Sponsors & Collaborators

  • Harran University

    collaborator OTHER
  • University of Cape Coast

    collaborator OTHER
  • Bielefeld University

    collaborator OTHER
  • Erzurum Technical University

    lead OTHER

Principal Investigators

  • Esedullah AKARAS, Dr. · Erzurum Technical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-03-01
Primary Completion
2026-04-15
Completion
2026-05-03

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07670793 on ClinicalTrials.gov