The Effect of Virtual Reality Headset and Hand Massage on Pain, Anxiety, Patient Satisfaction, and Physiological Parameters in Patients Who Have Undergone Abdominal Surgery
NCT07929337, Not applicable, Not yet recruiting, Dokuz Eylul University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | The Effect of Virtual Reality Headset and Hand Massage on Pain, Anxiety, Patient Satisfaction, and Physiological Parameters in Patients Who Have Undergone Abdominal Surgery | ClinicalTrials.gov |
| NCT number | NCT07929337 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 66 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Dokuz Eylul University | ClinicalTrials.gov |
| Conditions | Pain After Surgery, Pain and Anxiety, Anxiety After Surgery, Anxiety, Abdominal Surgery | ClinicalTrials.gov |
| Interventions | Virtual Reality Glasses, Classic Hand Massage | ClinicalTrials.gov |
| First posted | 2026-11-10 | ClinicalTrials.gov |
| Last updated | 2026-11-10 | ClinicalTrials.gov |
Registered outcomes 7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Postoperative pain | The second day after surgery, immediately before the procedure, immediately after the procedure, and 30 minutes later. | Pain intensity will be measured using a Visual Analog Scale (VAS) ranging from 0 (no pain) to 10 (the most severe pain possible). Measurements will be taken three times: on the second day after surgery, immediately before the procedure, immediately after the procedure, and 30 minutes later. | ClinicalTrials.gov |
| Secondary | Postoperative anxiety levels | The second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. | Anxiety levels will be assessed using the Situational Anxiety Inventory - Short Form (STAIS-S). This scale measures temporary anxiety levels. Scores range from 20 to 80. Measurements will be taken three times: on the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. Higher scores indicate higher (worse) anxiety levels. | ClinicalTrials.gov |
| Secondary | Post-surgery satisfaction levels | The second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. | Patient satisfaction will be assessed using a Visual Analog Scale (VAS) ranging from 0 (not at all satisfied) to 10 (extremely satisfied). Measurements will be taken three times: on the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. Higher scores indicate greater satisfaction. | ClinicalTrials.gov |
| Secondary | Systolic Blood Pressure | The second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. | Systolic blood pressure will be measured in millimeters of mercury (mmHg). Higher values indicate higher systolic blood pressure. | ClinicalTrials.gov |
| Secondary | Diastolic Blood Pressure | The second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. | Diastolic blood pressure will be measured in millimeters of mercury (mmHg). Higher values indicate higher diastolic blood pressure. | ClinicalTrials.gov |
| Secondary | Pulse Rate | The second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. | Pulse rate will be measured in beats per minute (beats/min). | ClinicalTrials.gov |
| Secondary | Respiratory Rate | The second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. | Respiratory rate will be measured in breaths per minute (breaths/min). | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)