Trial · NCT07887035
Reiki After Bariatric Surgery
NCT07887035, Not applicable, Completed, TC Erciyes University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Reiki After Bariatric Surgery. Trials, record NCT07887035. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07887035
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Reiki After Bariatric Surgery
- NCT number
- NCT07887035
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 75 participants, actual
- Lead sponsor
- TC Erciyes University
- Conditions
- Nausea and Vomitting, Distension; Bowel, Pain, Comfort
- Interventions
- reiki, Sham Reiki
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Nausea and Vomitting | Before Reiki administration and on postoperative days 0, 1, and 2. On the evening of discharge, the scale was administered by telephone on postoperative day 3. | Nausea was assessed using the Rhodes Index of Nausea, Vomiting, and Retching (INVR). The maximum possible score is 32, with higher scores indicating more severe nausea, vomiting, and retching symptoms. |
| Primary | Pain | Twice daily (before and after the intervention) for three postoperative days. | The Numerical Rating Scale (NRS) was used to assess pain intensity. Participants were informed that "0" represented "no pain at all," that pain intensity increased as the numbers increased, and that "10" represented "unbearable pain." They were then asked to select the number that best represented their pain intensity. |
| Primary | Distension | Twice daily (before and after the intervention) for three postoperative days. | The Numerical Rating Scale (NRS) was used to assess abdominal distension. Participants were informed that "0" represented "no abdominal distension," that the severity of abdominal distension increased as the numbers increased, and that "10" represented "the most severe abdominal distension imaginable." They were then asked to select the number that best represented their perceived level of abdominal distension. |
| Primary | Comfort | Twice daily (before and after the intervention) for three postoperative days. | Patient comfort was assessed using the General Comfort Questionnaire (GCQ). The maximum possible total score is 192, and the minimum is 48. |
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/NCT07887035
GET https://conductscience.org/api/trials/v1/NCT07887035/registered