MedPath

The Effect of Hot Foot Bath on Sleep Quality and Fatigue

Not Applicable
Not yet recruiting
Conditions
Hepatitis B
Registration Number
NCT06864923
Lead Sponsor
Uludag University
Brief Summary

This study will be conducted to investigate the effects of hot foot baths on patients' sleep quality and fatigue severity levels.The study will be conducted in the Gastroenterology clinic of a university hospital in Türkiye. The research sample will consist of 60 adult patients. Patients will be randomly divided into two groups: the intervention and control groups. The intervention group will receive hot foot baths for three consecutive nights starting from the second day of hospitalization. The foot bath will be applied one hour before the patient goes to bed at night. The foot tub will be filled with hot water to approximately 20 cm above the patient's ankle and the temperature of the water will be measured with a water thermometer. The temperature of the water will be kept stable at 41-42°C. This application will be done for 20 minutes. The sleep and fatigue levels of the patients will be measured with measurement tools in the morning (3 times) following each application. No application will be applied to the control group, and sleep and fatigue levels will be measured in a similar manner to the measurement tools applied to the intervention group and the application days.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • being over the age of 18,
  • having no disorder which could affect pain perception,
  • having no communication problem, and voluntarily agreeing to participate in the research,
  • Having been admitted to the clinic at least 24 hours ago,
  • Not having a diagnosed sleep disorder,
  • Not having a psychiatric disorder requiring treatment,
  • Not having a problem with vital signs before the application,
  • Not using narcotic drugs in the last 4 hours,
  • Not eating two hours before going to bed at night
Exclusion Criteria
  • being under the age of 18
  • not being conscious, refusing to participate in the research or opting to leave the study at any point,
  • Having a problem with vital signs before the application,
  • Having a diagnosed sleep disorder.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
fatigue severity in score (0-10)4 months

Brief Fatigue Inventory: Scoring ranges from "0" to "10", with "0" indicating no effect and "10" indicating the highest level of effect. The general fatigue score is calculated by dividing the total score of items 1, 2 and 3 by 3, and the effect score of fatigue on daily living activities is calculated by dividing the total score of items 4a, 4b, 4c, 4d, 4e and 4f by 6. A score of "0" obtained from the KYE indicates no fatigue, "1-3" indicates low fatigue, "4-6" indicates moderate fatigue, "7-9" indicates high fatigue and "10" indicates the highest level of effe

Sleep Quality in score4 months

Sleep Quality Scale: It consists of a total of 18 items. It includes items related to the sleep process and sleep satisfaction.

Secondary Outcome Measures
NameTimeMethod
weight4 months

weight in kilograms

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