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The Effect of Heating the Intensive Care Room in the Early Postoperative Period on Patient Outcomes

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this study was to evaluate the effect of heating the intensive care room in the early postoperative period on patient outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• The following criteria will be included in the sample:

• Patients who underwent elective abdominal surgery and were admitted to intensive care after surgery.

• Patients aged 18 and over.

• Patients whose body temperature on the morning of surgery was neither below 36°C nor above 37.5°C.

• Patients who did not have a pacemaker, dementia, advanced spasticity, muscle atrophy, peripheral lesions, osteoporosis, skin irritation, diabetes, hypertension, or obesity.

• Patients who did not require mechanical ventilation.

• Patients who did not have any illness that would impair thermoregulation (such as head trauma or hypothalamic damage).

• • Patients who were not taking medications that would affect thermoregulation, such as vasodilators.

• Patients who did not have peripheral circulation problems.

• Patients who were not alcohol or substance abusers.

• Patients who did not have mental retardation.

• Patients who were conscious and oriented to person, time, and place.

• Patients who could speak Turkish.

• Patients who did not have any auditory or visual impairments.

• Patients who volunteered for the study.

Locations
Other Locations
Turkey
Adana City Training and Research Hospital
RECRUITING
Adana
Contact Information
Primary
Cansel Bozer Uludağ, expert
cansel9815@gmail.com
+905434332624
Time Frame
Start Date: 2025-04-20
Estimated Completion Date: 2025-10-30
Participants
Target number of participants: 70
Treatments
No_intervention: no intervention group
In the preoperative period, patients with a body temperature of 36°C-37°C one hour before surgery will be included in the sample. Postoperatively, upon arrival from the operating room to the intensive care unit, which has a humidity range of 55%-65% and a temperature range of 22°C-25°C, will be safely transferred to a single-bed room, monitored, and wiped down. After ensuring personal hygiene, the patient will be covered with a 160x220cm cotton quilt. The heating device hose will be placed inside the bed from the side of the bed. The electric heater will be operated at 38°C (Medium) for 120 minutes, 15 cm from the patient's body. Routine treatment and care will then be administered. Vital signs, shivering level, and temperature perception will be recorded on the patient's follow-up form at 0, 15, 30, 45, 60, 90, and 120 minutes postoperatively.
Experimental: intervention group
In the preoperative period, patients with a body temperature of 36°C to 37°C one hour before surgery will be included in the sample. In the postoperative period, the intensive care room, which has a routine humidity range of 55%-65% and a temperature of 22°C to 25°C, will be heated to the upper limit of the intensive care room temperature range, 27°C, with an electric heater half an hour before the operation. After ensuring personal hygiene, the patient will be safely transferred to the bed in the single room, monitored, and wiped down. After ensuring personal hygiene, the patient will be covered with a 160x220cm cotton quilt. The heating device hose will be placed inside the bed from the edge of the bed. The electric heater will be operated at 38°C (Medium Level) for 120 minutes, 15cm from the patient's body. Routine treatment and maintenance will be administered. Then, the vital signs, pain, shivering level, and temperature perception will be recorded in the patient follow-up form a
Related Therapeutic Areas
Sponsors
Leads: Cukurova University

This content was sourced from clinicaltrials.gov