Trial · NCT07880587
Reflexology Hand Massage After Cesarean Section
NCT07880587, Not applicable, Recruiting, Dokuz Eylul University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Reflexology Hand Massage After Cesarean Section. Trials, record NCT07880587. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07880587
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Reflexology Hand Massage After Cesarean Section
- NCT number
- NCT07880587
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 40 participants, estimated
- Lead sponsor
- Dokuz Eylul University
- Conditions
- Cesarean Section, Anxiety, Postoperative Period
- Interventions
- Reflexology Hand Massage, Stroking Hand Massage
- First posted
- 2026-10-19
- Last updated
- 2026-10-19
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in State Anxiety Levels | Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage. | Anxiety will be assessed using the State Anxiety Inventory (STAI). The state subscale consists of 20 items rated on a 4-point Likert scale. Total scores range from 20 to 80. Higher scores indicate higher levels of state anxiety. |
| Secondary | Change in Patient Satisfaction | Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage. | Patient satisfaction will be evaluated using a Visual Analog Scale (VAS). The scale is a 10-centimeter line ranging from 0 to 10, where 0 represents 'completely dissatisfied' and 10 represents 'completely satisfied.' Higher scores indicate greater satisfaction with the postoperative care. |
| Secondary | Change in Hemodynamic Parameters1 | 1 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage. | Physiological evaluation will include the measurement of systolic blood pressure (mmHg), diastolic blood pressure (mmHg) |
| Secondary | Change in Hemodynamic Parameters 2 | 2 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage. | Physiological evaluation will include the measurement of heart rate (beats per minute) |
| Secondary | Change in Hemodynamic Parameters 3 | 3 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage. | Physiological evaluation will include the measurement of respiratory rate (breaths per minute) |
| Secondary | Change in Hemodynamic Parameters 4 | 4 Baseline (before the intervention at the 4th postoperative hour) and 30 minutes after the completion of the 20-minute massage. | Physiological evaluation will include the measurement of peripheral oxygen saturation (SpO2, %). |
Source ClinicalTrials.gov
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.
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/NCT07880587
GET https://conductscience.org/api/trials/v1/NCT07880587/registered