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mandala: Mandala Intervention on Mental Distress in Nurses Working With Terminally Ill Patients

Sponsor
Istanbul Sabahattin Zaim University (Other)
Overall Status
Completed
CT.gov ID
NCT05444010
Collaborator
(none)
56
Enrollment
2
Locations
1
Arm
1.2
Actual Duration (Months)
28
Patients Per Site
23.7
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Mandala application intervention of mental distress in nurses working with terminally ill patients

Condition or Disease Intervention/Treatment Phase
  • Behavioral: mandala painting
 N/A

Detailed Description

Questionnaires were applied to the control and experimental groups. Mandala painting was done to the experimental group. Questionnaires were applied to the control and experimental groups again. Distress, anxiety, depression, death anxiety, death depression and psychological well-being of the experimental and control groups were evaluated.

Study Design

Study Type:
Interventional
Actual Enrollment :
56 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
This study is an experimental study with pre-test and post-test control grupsThis study is an experimental study with pre-test and post-test control grups
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Mandala Intervention on Mental Health Problems of Nurses Caring for Terminally Ill Patients
Actual Study Start Date :
May 15, 2022
Actual Primary Completion Date :
Jun 15, 2022
Actual Study Completion Date :
Jun 20, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: mental health

The effect of mandala painting on mental health. Mental health-related anxiety, depression, well-being, distress and death anxiety and depression will be measured.

Behavioral: mandala painting
nurse painted mandala for relaksing

Outcome Measures

Primary Outcome Measures

  1. Beck depresion scale [4 week]

    depresion is mental breakdown, depresion for beck depresion scale, 0-9 depresion emity, 10-15 light depression, 16-23 middle depresion, 24- 63 severe depression

Secondary Outcome Measures

  1. STAI-trait anxiety scale [4 week]

    anxiete is boredom, anxiete for trait anxiety scale, 0-15 anxiety none,n , 15-30 light anxiety, 30-60 middle anxiety, over 60 severe anxiety

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

volunteer

  • active employee

  • year of study

Exclusion Criteria:

  • paint allergy

  • use of psychiatric drugs Loss of loved one in the last six months

Contacts and Locations

Locations

Site City State Country Postal Code
1 SZU Istanbul İSTANBUL/halkalı Turkey 34000
2 SZU Istanbul İ̇stanbul Turkey 34000

Sponsors and Collaborators

  • Istanbul Sabahattin Zaim University

Investigators

  • Study Director: RUKİYE PINAR BÖLÜKTAŞ, SZU

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Arzu Nurdaş, Principal investigator, Istanbul Sabahattin Zaim University
ClinicalTrials.gov Identifier:
NCT05444010
Other Study ID Numbers:
  • ISZU
First Posted:
Jul 5, 2022
Last Update Posted:
Jul 28, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Arzu Nurdaş, Principal investigator, Istanbul Sabahattin Zaim University
mental health, anxiety, depression

Study Results

No Results Posted as of Jul 28, 2022