ClinicalTrials.Veeva

Menu

Orenage Blossom Oil Essential Application in Stoma (Stoma Care)

Ç

Çukurova University

Status

Not yet enrolling

Conditions

Stoma
Nursing
Essential Oil
Nursing Care

Treatments

Behavioral: Essential Oil

Study type

Interventional

Funder types

Other

Identifiers

NCT07195136
06.09.2024/145
Cukurova University

Details and patient eligibility

About

Because the stoma will become a part of the individual's body and directly impact their quality of life, careful attention should be paid to its location and surgical procedure. Stoma care nurses should provide effective training to patients and those responsible for their care. Patients and their families should be regularly monitored, followed up, and cared for at home after discharge. They should also be provided with information about appropriate units to consult if any problems arise. Stoma support groups should be established to foster social interaction. A well-planned surgical procedure protects individuals from the development of complications and problems that can be considered a "life sentence."

Full description

This prospective, randomized, controlled study aims to investigate the effects of orange blossom essential oil placed in the stoma bag on odor reduction, social isolation, and stoma compliance in individuals with permanent colostomies. Sample size calculations were performed using a priori power analysis (t-test) for the intervention and control groups. Accordingly, with an effect size of d=1.12, a 5% error rate (α=0.05), and 80% power (1-β=0.80), the minimum sample size for both groups was calculated as 54. Considering potential losses, the total sample size will be increased by 10%, with 30 patients in each group (Experimental Group: 30, Control Group: 30), for a total of 60 patients. Data will be collected using a patient personal information form, a patient information form, a compliance scale for individuals with stoma, and a social isolation scale, all prepared by the researchers based on literature.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volunteer to participate in the study
  • Over 18 years of age
  • With a stoma
  • No stoma-related complications

Exclusion criteria

  • Leaving the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

intervention
Experimental group
Description:
essential oil
Treatment:
Behavioral: Essential Oil
control
No Intervention group
Description:
standart care

Trial contacts and locations

0

Loading...

Central trial contact

Meltem Akbaş, PhD; Meltem Akbas, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems