Orenage Blossom Oil Essential Application in Stoma

NCT07195136 — Not applicable, Completed, 60 participants, Cukurova University

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

Investigation of the Effect of Orange Blossom Essential Oil Placed in the Stoma Bag on Odor Removal, Social Isolation, and Stoma Adaptation in Individuals With Stoma

RegistryNCT07195136, acronym Stoma Care
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, supportive care
Enrollment60 (Actual)
SponsorCukurova University (Other)
ConditionsStoma, Nursing, Nursing Care, Essential Oil
InterventionsEssential Oil (Behavioral)
Datesstart 2025-09-18, primary completion 2025-10-01, completion 2025-11-01, first posted 2025-09-26, last updated 2026-03-20
Locations1 site in Turkey (Türkiye)

Related Papers Related Patents Related Grants Related Experts
All trials for Stoma All trials for Nursing All trials of Essential Oil

-Summary

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."

Expand all sections  ·  Collapse all

+Detailed 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.

+Arms and interventions

ArmTypeInterventionsDescription
interventionExperimentalBehavioral: Essential Oilessential oil
controlNo interventionstandart care
  • Essential Oil (Behavioral): essential oil

+Outcome measures

Primary outcomes

  • Stoma Adaptation Scale [30 day]: Scale items are scored between 0 and 4. The minimum score is 0 and the maximum is 92. A higher score indicates greater compliance with the stoma.
  • Social Isolation Scale [30 day]: Scale items are scored on a 1-3 scale. The minimum score is 14 and the maximum is 42. As the score increases, the level of social isolation increases.

+Eligibility

Sex: All, ages: 18 Years to any, 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

+Locations (1)

FacilityCityCountryStatus
Cukurova UniversityAdana, AdanaTurkey (Türkiye)

+Investigators

  • Meltem Akbaş, Principal investigator, Universty Of Cukurova