Reflexology Massage and Hot Water Foot Bath for Pain and GI Recovery After Colorectal Surgery
NCT ID: NCT06972199
Last Updated: 2025-05-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
102 participants
INTERVENTIONAL
2024-10-30
2026-06-30
Brief Summary
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Based on the percentage measurement values of the methods to be studied in the literature review, G-POWER programme was used for sample calculation with an effect size of 0.4 (Cohen), 95% power and 0.05% margin of error. Cohen\'s standard effect size was taken as the basis for the effect size. The calculated value is the total value for 3 groups and the total sample size for 3 groups was found as n=102. The number of samples per group was determined as (n)=34. In order to prevent bias in the study, patients who meet the study criteria will be distributed to the experimental and control groups by computerised randomisation programme. Data will be collected by using the Patient Information Form consisting of two parts, Rhodes Nausea, Vomiting and Retching Index and Numerical Proportioning Scale (NRS) developed by the researcher in line with the literature. The data obtained will be evaluated with appropriate statistical methods in the licensed SPSS 21.0 package programme.
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Detailed Description
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* Sociodemographic characteristics
* Medical and surgical history
* Postoperative vital signs (blood pressure, pulse, temperature, etc.)
* Gastrointestinal follow-up (bowel sounds per minute, time of first gas and feces output) This form was developed based on current literature and clinical practice guidelines and piloted prior to study launch. All data will be analyzed using SPSS 21.0.
The sample size was calculated using G\*Power based on an effect size of 0.4 (Cohen), 95% power, and a 0.05 margin of error, resulting in 102 total participants (n=34 per group).
Ethical approval was obtained from the Non-Interventional Clinical Research Ethics Committee of Fenerbahçe University. The study is being conducted at the General Surgery Clinic of SBÜ Ümraniye Training and Research Hospital.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Reflexology
Reflexology application
Reflexology
Reflexology application
Hot water foot bath
Hot water foot bath application
Hot water foot bath
Hot water foot bath application
Control
There will be no intervention
No interventions assigned to this group
Interventions
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Reflexology
Reflexology application
Hot water foot bath
Hot water foot bath application
Eligibility Criteria
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Inclusion Criteria
* Planning laparoscopic surgery for a malignant tumour in the large intestine,
* The same method was used for preoperative bowel and GI tract preparation,
* Postoperative Numerical Proportioning Scale (NRS) score of 3 and above,
* Verbal and written acceptance to participate in the research.
Exclusion Criteria
* Having a history of reflexology application before,
* Open wound, infection, circulatory disorder, lesion, etc. in the areas where reflexology massage or hot water foot bath will be applied,
* Patient-controlled analgesia in the early postoperative period
* Having any problem that prevents verbal communication.
18 Years
ALL
No
Sponsors
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Istanbul University - Cerrahpasa
OTHER
Responsible Party
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Cansu Mert
Doctoral Student
Principal Investigators
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Cansu Mert, Master
Role: PRINCIPAL_INVESTIGATOR
Istanbul University - Cerrahpasa
Locations
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Istanbul University-Cerrahpaşa
Istanbul, Istanbul, Turkey (Türkiye)
University of Health Sciences, Umraniye Training and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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18.2024fbu
Identifier Type: -
Identifier Source: org_study_id
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