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Clinical Trials/NCT06840171
NCT06840171CompletedNot Applicable

The Effect of Mandala Coloring on Depression, Anxiety and Quality of Life of Inpatients in a Psychiatric Clinic

reyhan eskiyurt1 site in 1 country51 target enrollmentStarted: February 22, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
51
Locations
1
Primary Endpoint
Depression-Anxiety-Stress Scale

Study Overview

Brief Summary

The aim of this study is to examine the effects of mandala coloring activity applied to individuals hospitalized in a psychiatric clinic with a diagnosis of anxiety and depression disorder on quality of life, psychological resilience and depression, anxiety and stress levels.

Detailed Description

Introduction

It is stated that healthcare professional-patient interaction and patient activity improve clinical outcomes for patients with mental illness. When compared to psychosocial interventions, the most commonly used method in 49% of clinics was found to be artistic practices. It is stated that mandala painting has a calming and healing effect on the individual, facilitating psychological integration and personal meaning in life.

Objective

The aim of this study is to examine the effects of mandala coloring activity applied to individuals hospitalized in a psychiatric clinic with a diagnosis of anxiety and depression disorder on quality of life, psychological resilience and depression, anxiety and stress levels.

Method: The research will be conducted using a randomized controlled experimental research design. The research sample will consist of 50 patients in a university hospital psychiatry clinic. Research data will be collected using the Introductory Information Form, Depression-Anxiety-Stress Scale Short Form, Quality of Life Scale (SF-12), and Brief Resilience Scale. Patients diagnosed with anxiety and depression will undergo 8 sessions of mandala application. Data will be collected in two time periods before starting the mandala application and at the end of the 8-session application.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Agreeing to participate in the study
  • •Being 18 years of age or older
  • •Diagnosed with anxiety and depression disorder

Exclusion Criteria

  • •Those who gave incomplete answers to the scales used in the study
  • •Those with serious psychiatric symptoms (e.g. harming themselves or others, sedation)
  • •Those who did not participate in the mandala coloring session
  • •Those who did not agree to participate in the study

Arms & Interventions

Experimental (mandala coloring)

Experimental

Mandala group will participate in 8 sessions of mandala application. Mandala Coloring Application will be applied to the Intervention group 2-3 times a week for 3 weeks. Mandala application will be done by the researcher and feedback about the mandala will be received from the patients at the end of each session. Data collection forms will be applied before the mandala painting application starts and after the mandala painting application ends (after the 8th session).

Intervention: Mandala coloring (Other)

Control

No Intervention

No intervention will be applied to the patients in the control group during the follow-up period, only data collection forms will be applied.

Outcomes

Primary Outcomes

Depression-Anxiety-Stress Scale

Time Frame: 3 week

The scale, developed to determine the depression, anxiety and stress levels of individuals, consists of 21 items and 3 subscales. Depression-Anxiety-Stress Scale is a 4-point Likert-type measurement tool (0-not suitable for me and 3-completely suitable for me). The Turkish validity and reliability study of Depression-Anxiety-Stress Scale was conducted. High scores on the scale reveal which of the depression, anxiety and stress sub-dimensions the individual is experiencing problems with.

Quality of Life Scale

Time Frame: 3 week

Quality of life scale (The SF-12) has two summary scales: physical component and mental component. The physical component summary scale consists of physical function, physical role, body pain and general health subscales, and the mental component summary consists of vitality, social function, emotional role and mental health subscales. The score of each subscale varies between 0-100 and the score is directly proportional to the quality of life. The Turkish validity and reliability study of the scale was conducted. Minimum and maximum scores can range from 0-100 from the scale. High scores indicate high quality of life.

Brief Psychological Resilience Scale

Time Frame: 3 week

Brief Psychological Resilience Scale is a 5-point Likert-type, 6-item, self-report measurement tool. After the reverse-coded items in the scale are translated, high scores indicate high psychological resilience. The Turkish validity and reliability study of the scale.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
reyhan eskiyurt
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

reyhan eskiyurt

Director

Ankara Yildirim Beyazıt University

Study Sites (1)

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