Trial · NCT07886736
Acute Effects of Stretching, Kinesio Taping, Cold Water Immersion and Foam Rolling on Wrist Strength and Precise Force and Position Control
NCT07886736, Not applicable, Completed, Grgur Kovačić
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Acute Effects of Stretching, Kinesio Taping, Cold Water Immersion and Foam Rolling on Wrist Strength and Precise Force and Position Control. Trials, record NCT07886736. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07886736
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Acute Effects of Stretching, Kinesio Taping, Cold Water Immersion and Foam Rolling on Wrist Strength and Precise Force and Position Control
- NCT number
- NCT07886736
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 56 participants, actual
- Lead sponsor
- Grgur Kovačić
- Conditions
- Healthy Volunteers, Muscle Strength, Motor Control
- Interventions
- Static stretching, Assisted dynamic stretching, Kinesio taping, Cold water immersion, Foam rolling
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Peak Isometric Wrist-Flexion Force | Pre-intervention and 10-20 seconds post-intervention at each of 5 intervention visits (Weeks 2-6) | Peak force (newtons), defined as the highest 1-second moving average of the force signal in the best of three maximal isometric wrist-flexion contractions. Change is expressed as the percentage change from pre- to post-intervention. |
| Primary | Change in Normalised Error of the Force-Tracking Task | Pre-intervention and approximately 3-6 minutes post-intervention at each of 5 intervention visits (Weeks 2-6) | Normalised error (%) while tracking a randomly generated sinusoidal force curve with isometric wrist flexion, calculated as the root-mean-square deviation from the reference curve divided by its amplitude and averaged over three trials. Change is expressed as the percentage change from pre- to post-intervention. |
| Primary | Change in Normalised Error of the Position-Tracking Task | Pre-intervention and approximately 8-11 minutes post-intervention at each of 5 intervention visits (Weeks 2-6) | Normalised error (%) while tracking a randomly generated sinusoidal wrist-angle curve with wrist flexion and extension, calculated as the root-mean-square deviation from the reference curve divided by its amplitude and averaged over three trials. Change is expressed as the percentage change from pre- to post-intervention. |
| Secondary | Change in Active Palmar-Flexion Range of Motion | Pre-intervention and approximately 6-8 minutes post-intervention at each of 5 intervention visits (Weeks 2-6) | Active range of palmar flexion (degrees), measured once with the built-in goniometer of the measurement system. |
| Secondary | Change of Tracking Error Across Visits in the Pre-intervention Measurements (Learning) | Pre-intervention at each of 6 weekly visits (Weeks 1-6) | Slope of the normalised error of both tracking tasks across visits (percentage change per visit) from a linear mixed model of the log value. |
| Secondary | Change in Mean Absolute Error of the Force-Tracking Task | Pre-intervention and approximately 3-6 minutes post-intervention at each of 5 intervention visits (Weeks 2-6) | Mean absolute deviation (newtons) of the produced force from the reference curve, averaged over three trials. Change is expressed as the percentage change from pre- to post-intervention. |
| Secondary | Change in Mean Absolute Error of the Position-Tracking Task | Pre-intervention and approximately 8-11 minutes post-intervention at each of 5 intervention visits (Weeks 2-6) | Mean absolute deviation (degrees) of the produced wrist angle from the reference curve, averaged over three trials. Change is expressed as the percentage change from pre- to post-intervention. |
| Secondary | Change in Peak Force by Repetition Position | Pre-intervention and 10-20 seconds post-intervention at each of 5 intervention visits (Weeks 2-6) | Percentage change in peak force (newtons) from pre- to post-intervention, calculated separately for the first, second and third maximal contraction of the measurement block. |
| Secondary | Within-Session Intraclass Correlation Coefficient | 11 measurement occasions over 6 weeks (Weeks 1-6) | Intraclass correlation coefficient, ICC(3,1), across the three trials within each measurement occasion (unitless), reported separately for peak force and for the normalised errors of the two tracking tasks. |
| Secondary | Between-Visit Intraclass Correlation Coefficient | Pre-intervention at each of 6 weekly visits (Weeks 1-6) | Intraclass correlation coefficient, ICC(3,1), of the pre-intervention values across the six visits (unitless), reported separately for peak force and for the normalised errors of the two tracking tasks. |
1 to 10 of 15Source ClinicalTrials.gov
See all 15 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/NCT07886736
GET https://conductscience.org/api/trials/v1/NCT07886736/registered