Trial · NCT07904858
Soft Tissue Relaxation in Trumpet Players
NCT07904858, Not applicable, Completed, National Taipei University of Nursing and Health Sciences
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Soft Tissue Relaxation in Trumpet Players. Trials, record NCT07904858. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07904858
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Soft Tissue Relaxation in Trumpet Players
- NCT number
- NCT07904858
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 15 participants, actual
- Lead sponsor
- National Taipei University of Nursing and Health Sciences
- Conditions
- Healthy Volunteers, Muscle Tension
- Interventions
- Integrated soft tissue relaxation (IASTM + manual release)
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Forced Vital Capacity (FVC) | Baseline (immediately before) and immediately after the single intervention session (same day) | FVC in liters (L), measured with a CHEST HI-801 spirometer. |
| Primary | Resting Minute Ventilation | Baseline (immediately before) and immediately after the single intervention session (same day) | Minute ventilation during quiet breathing in liters per minute (L/min), measured with a CHEST HI-801 spirometer. |
| Primary | Forced Expiratory Volume in 1 Second (FEV1) | Baseline (immediately before) and immediately after the single intervention session (same day) | FEV1 in liters (L), measured with a CHEST HI-801 spirometer. |
| Primary | Peak Expiratory Flow (PEF) | Baseline (immediately before) and immediately after the single intervention session (same day) | PEF in liters per second (L/s), measured with a CHEST HI-801 spirometer. |
| Primary | Maximal Voluntary Ventilation (MVV) | Baseline (immediately before) and immediately after the single intervention session (same day) | MVV in liters per minute (L/min), measured with a CHEST HI-801 spirometer. |
| Primary | Resting Tidal Volume | Baseline (immediately before) and immediately after the single intervention session (same day) | Tidal volume during quiet breathing in liters (L), measured with a CHEST HI-801 spirometer. |
| Primary | Resting Respiratory Rate | Baseline (immediately before) and immediately after the single intervention session (same day) | Respiratory rate during quiet breathing in breaths per minute, measured with a CHEST HI-801 spirometer. |
| Primary | Ventilatory Reserve | Baseline (immediately before) and immediately after the single intervention session (same day) | Ventilatory reserve in percent (%), calculated by the CHEST HI-801 spirometer from resting minute ventilation relative to MVV. |
| Secondary | Standard Deviation of Fundamental Frequency During Sustained Note | Baseline (immediately before) and immediately after the single intervention session (same day) | Standard deviation of the fundamental frequency in hertz (Hz) during a sustained G4 note, extracted with automated pYIN-based acoustic analysis. |
| Secondary | Mean Fundamental Frequency During Sustained Note | Baseline (immediately before) and immediately after the single intervention session (same day) | Mean fundamental frequency in hertz (Hz) during a sustained G4 note, extracted with automated pYIN-based acoustic analysis. |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT07904858
GET https://conductscience.org/api/trials/v1/NCT07904858/registered