Trial · NCT07904520
Abdominal Massage and Range-of-motion Exercise in Enterally Fed ICU Patients With Pressure Injuries
NCT07904520, Not applicable, Completed, Bartın Unıversity
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Abdominal Massage and Range-of-motion Exercise in Enterally Fed ICU Patients With Pressure Injuries. Trials, record NCT07904520. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07904520
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Abdominal Massage and Range-of-motion Exercise in Enterally Fed ICU Patients With Pressure Injuries
- NCT number
- NCT07904520
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 90 participants, actual
- Lead sponsor
- Bartın Unıversity
- Conditions
- Critical Illness, Pressure Injuries, Enteral Nutrition Intolerance in Critically Ill Patients
- Interventions
LAM group, Intervention and control-group data were collected daily at 10:00 AM. In the intervention groups, each 15-minute session was followed by outcome measurements the next day before the following session,, ROM, Control
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in total score on the Pressure Ulcer Scale for Healing (PUSH) of the first (largest) pressure injury | Baseline and daily for 7 days | Pressure injury healing will be measured with the Pressure Ulcer Scale for Healing (PUSH), version 3.0, which combines wound surface area (length × width), exudate amount and tissue type into a total score. Unit of measure: score on a scale (range 0-17; higher scores indicate a worse wound status). The change from baseline to Day 7 will be reported for the first (largest) pressure injury of each participant. |
| Secondary | Change in total PUSH score of the second pressure injury | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: score on a scale (PUSH total score, range 0-17; higher scores indicate a worse wound status). Measured with the Pressure Ulcer Scale for Healing (PUSH) in participants who have a second pressure injury. |
| Secondary | Change in total PUSH score of the third pressure injury | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: score on a scale (PUSH total score, range 0-17; higher scores indicate a worse wound status). Measured with the Pressure Ulcer Scale for Healing (PUSH) in participants who have a third pressure injury. |
| Secondary | Percentage of participants with defecation | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: percentage of participants who had at least one bowel movement in the preceding 24 hours, recorded daily by the researcher on the Intervention/Control Group Patient Monitoring Form (nursing observation/chart record). |
| Secondary | Percentage of participants with nausea or vomiting Baseline and daily for 7 | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: percentage of participants with nausea and/or vomiting episodes in the preceding 24 hours, recorded daily on the Patient Monitoring Form by nursing observation. |
| Secondary | Percentage of participants with abdominal distension | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: percentage of participants with abdominal distension, assessed daily by clinical observation/palpation of the abdomen by the researcher and recorded on the Patient Monitoring Form. |
| Secondary | Gastric residual volume | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: millilitres (mL). Gastric residual volume is aspirated through the nasogastric tube with a syringe between 02:00 and 04:00 when enteral feeding is paused, and recorded daily. |
| Secondary | Serum albumin concentration | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: concentration in grams per litre (g/L). Serum albumin is measured by the hospital laboratory from routine venous blood samples and recorded daily from the patient file. |
| Secondary | Enteral feeding flow rate | Baseline and daily for 7 days (Day 1 to Day 7) | Unit of measure: millilitres per hour (mL/h). The formula infusion rate is read from the enteral feeding pump/order and recorded daily. (Enteral water flow rate, also in mL/h, may be added as a separate outcome if desired.) |
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/NCT07904520
GET https://conductscience.org/api/trials/v1/NCT07904520/registered