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Clinical Trials/NCT05367414
NCT05367414
Completed
N/A

The Effect of Aromatherapy Massage on Itching, Comfort, Skin PH Level, and Skin Moisture in Liver Diseases: Randomised Controlled Trial

Amine Terzi1 site in 1 country36 target enrollmentFebruary 13, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Amine Terzi
Enrollment
36
Locations
1
Primary Endpoint
Itching
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of this study is to determine the effect of aromatherapy massage on itching, comfort, skin pH level and skin moisture in individuals with liver disease.

Research Hypotheses:

H1: Aromatherapy massage has an effect on the level of itching in individuals with itchy liver disease.

H2: Aromatherapy massage has an effect on the general comfort level in individuals with itchy liver disease, H3: Aromatherapy massage has an effect on skin pH level in individuals with itchy liver disease.

H4: Aromatherapy massage has an effect on skin moisture in individuals with itchy liver disease.

Detailed Description

This randomised controlled trial was conducted in order to examine study effect of aromatherapy massage on itching, comfort, skin pH level, and skin moisture among individuals with liver diseases

Registry
clinicaltrials.gov
Start Date
February 13, 2020
End Date
June 23, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amine Terzi
Responsible Party
Sponsor Investigator
Principal Investigator

Amine Terzi

Asst. Prof.

Artvin Coruh University

Eligibility Criteria

Inclusion Criteria

  • patients who volunteered to participate in the study,
  • with a diagnosis of chronic liver disease (liver cirrhosis (primary biliary cirrhosis, alcoholic, cardiac, post-necrotic, cryptogenic cirrhosis, Wilson's Cirrhosis, hemochromatosis), chronic viral hepatitis),
  • had no cognitive impairment,
  • were not included in the pre-application,
  • could answer questions,
  • itch score of above 3 (with Visual Analogue Scale).

Exclusion Criteria

  • patients are taking antipruritic treatment,
  • have itchy skin disease before, ulcer, eczema, etc. in the area to be applied
  • patients with dermatological problems, any swelling or signs of inflammation in the area ---to be treated, neuropathy or loss of sensation in the area to be treated
  • patients with allergic to tea tree oil, perfume, or cosmetics,
  • diagnosed with cancer

Outcomes

Primary Outcomes

Itching

Time Frame: Day 14

Itching was assessed with the 5D Itch Scale. The total score of the scale ranges from 5 to 25, with 5 points indicating the absence of itching and 25 points indicating the highest severity of itching.

skin moisture level

Time Frame: Day 14

DMM brand skin moisture measuring device was used to measure skin moisture level.

skin pH level

Time Frame: Day 14

For pH level measurement, the F-74 G model skin pH measuring device manufactured by HORIBA Scientific and ISFET (Ion Sensitive Field Effect Transistor) 0040-10D model pH electrode produced by HORIBA Scientific were used.

comfort

Time Frame: Day 14

Comfort assessed with the General Comfort Scale. The score to be obtained from the scale varies between 48 and 192. 48 points indicating the low comfort level and 192 points indicating the high comfort level.

Study Sites (1)

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