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Heat Application on Gastrointestinal System Functions

The Effect of Heat Application on Gastrointestinal System Functions in Patients Receiving Continuous Enteral Nutrition

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06225687
Enrollment
60
Registered
2024-01-26
Start date
2024-02-01
Completion date
2024-12-01
Last updated
2024-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Enteral Nutrition, Gastrointestinal System--Abnormalities

Keywords

Enteral Nutrition, Heat Application, Gastrointestinal System Functions, Continuous Enteral Nutrition

Brief summary

Complications related to the gastrointestinal system can occur in patients receiving enteral nutrition. These complications may include nausea, vomiting, diarrhea, constipation, decreased bowel sounds, abdominal distension, increased gastric residual volume, and abdominal pain. To prevent and treat food intolerance, as well as to increase gastric emptying, the use of prokinetic agents is often preferred. However, these drugs have various side effects, such as abdominal cramps, allergies, bronchospasm, cardiac issues, and pancreatic disorders. One non-pharmacological method that can be applied to increase bowel motility and reduce abdominal distension and constipation is heat application. The aim of this study is to determine the effect of heat application to the abdominal and lumbar regions, using a hot water bag, on gastrointestinal system functions in patients receiving continuous enteral nutrition.

Interventions

The researcher will conduct daily measurements of gastric residual volume (GRV) and abdominal circumference, listen to bowel sounds, and assess distension from the first day of enteral nutrition initiation. Additionally, they will record the frequency of vomiting/defecation. Subsequently, a 15-minute hot application will be applied to the abdominal/lumbar region.

Sponsors

TC Erciyes University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Intensive care unit patients * Individuals aged 18 and above * Patients receiving enteral nutrition via nasogastric tube * Patients on the first day of enteral nutrition * Those receiving standard enteral nutrition solution * Patients without wounds in the abdominal region * Individuals who have not undergone abdominal surgery in the last 6 months * Patients not undergoing radiation/chemotherapy * Those with a high-output fistula without ileus problems * Patients without diarrhea and constipation * Patients with a Glasgow Coma Scale (GKS) \> 3 * Those with an APACHE II score \> 16 * Patients not taking prokinetic agents * Patients not taking laxative medications * Patients without any contraindications for the application of heat, such as neuropathy (to be determined in consultation with the primary doctor).

Exclusion criteria

* Patients in whom enteral nutrition is discontinued during the study * Patients transitioning to a product other than the standard one in enteral nutrition * Patients who temporarily pause enteral nutrition * Patients who have started prokinetic agents * The study will be terminated in patients who have started taking laxative medications.

Design outcomes

Primary

MeasureTime frameDescription
Gastric residual volume7 daysGRV measurement will be made 30 minutes after stopping feeding. It will be evaluated before and after application.
Abdominal Distension7 daysAbdominal distension will be assessed 30 minutes after stopping feeding. The palpation method will be used. Additionally, abdominal circumference will be measured with a tape measure. Evaluation will be made before and after the intervention.
Bowel sounds7 daysBowel sounds should be evaluated 30 minutes after stopping feeding. Bowel sounds are listened to with a stethoscope for one minute. It will be evaluated before and after the intervention.

Secondary

MeasureTime frameDescription
Defecation Patterns7 daysmeasure defecation frequency and nature
Vomiting7 daysThe number of vomitings during the day is recorded

Contacts

Primary ContactÖzlem Ceyahn
ozlemg@erciyes.edu.tr+903522076666

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026