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Trial · NCT07912580

Acute Effects of Shoulder Dynamic Taping in Competitive Volleyball Players

NCT07912580, Not applicable, Completed, Balikesir University

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Acute Effects of Shoulder Dynamic Taping in Competitive Volleyball Players. Trials, record NCT07912580. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07912580

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Acute Effects of Shoulder Dynamic Taping in Competitive Volleyball Players
NCT number
NCT07912580
Status
Completed
Phases
Not applicable
Enrollment
30 participants, actual
Lead sponsor
Balikesir University
Conditions
Athletic Performance, Shoulder Muscle Strength, Taping
Interventions
Dynamic shoulder taping, Sham shoulder taping
First posted
2026-11-03
Last updated
2026-11-03

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryServe Velocity
During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Serve velocity was measured using a handheld radar gun (Bushnell Speed Radar Gun, Model 101911). Participants performed three successful maximal-effort serves under both taped and untaped conditions. The mean velocity of the three successful serves was calculated for each condition. Serve velocity was recorded in kilometers per hour (km/h).
SecondaryIsometric Shoulder Internal Rotation Strength
During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Isometric shoulder internal rotation strength was measured on the dominant arm using a MicroFET2 handheld dynamometer. Participants were positioned prone with the shoulder abducted to 90° and elbow flexed to 90°. Three maximal isometric contractions were performed using the break-test method, with 1-minute rest intervals. The mean peak force of the three trials was recorded in kilograms-force (kgf). Higher values indicate greater muscle strength.
SecondaryIsometric Shoulder External Rotation Strength
During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Isometric shoulder external rotation strength was measured on the dominant arm using a MicroFET2 handheld dynamometer. Participants were positioned prone with the shoulder abducted to 90° and elbow flexed to 90°. Three maximal isometric contractions were performed using the break-test method, with 1-minute rest intervals. The mean peak force of the three trials was recorded in kilograms-force (kgf). Higher values indicate greater muscle strength.
SecondaryFunctional Throwing Performance Index (FTPI)
During a single assessment session, in randomized order: (1) untaped assessment, either before tape application or 45 minutes after tape removal following a washout period; and (2) taped assessment, 45 minutes after tape application.
Functional throwing performance was assessed using the Functional Throwing Performance Index (FTPI). Participants repeatedly threw a ball at a 30 × 30 cm target positioned 120 cm above the floor from a distance of 4.5 m for 30 seconds. FTPI was calculated as the percentage of successful throws relative to the total number of throws. Three trials were performed with 1-minute rest intervals, and the mean FTPI percentage was used for analysis. Higher scores indicate greater throwing accuracy.
SecondaryAthlete Satisfaction With TapingOnce, immediately after completion of all performance assessments (Day 1).
Athlete satisfaction with the assigned taping intervention was assessed once after completion of all performance assessments. Participants rated their overall satisfaction specifically with the taped condition using a study-specific, single-item, 11-point numerical rating scale ranging from 0 (not satisfied at all) to 10 (completely satisfied). Higher scores indicate greater satisfaction with the taping intervention.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
39180114RESULT

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07912580

GET https://conductscience.org/api/trials/v1/NCT07912580/registered