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

July 26, 2022 updated by: Arzu Nurdaş, Istanbul Sabahattin Zaim University

Mandala Intervention on Mental Health Problems of Nurses Caring for Terminally Ill Patients

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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 Type

Interventional

Enrollment (Actual)

56

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
    • İSTANBUL/halkalı
      • Istanbul, İSTANBUL/halkalı, Turkey, 34000
        • SZU
    • İ̇stanbul
      • Istanbul, İ̇stanbul, Turkey, 34000
        • SZU

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 50 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Beck depresion scale
Time Frame: 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
4 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
STAI-trait anxiety scale
Time Frame: 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
4 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Istanbul Sabahattin Zaim University

Investigators

  • Study Director: RUKİYE PINAR BÖLÜKTAŞ, SZU

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 15, 2022

Primary Completion (ACTUAL)

June 15, 2022

Study Completion (ACTUAL)

June 20, 2022

Study Registration Dates

First Submitted

June 16, 2022

First Submitted That Met QC Criteria

June 30, 2022

First Posted (ACTUAL)

July 5, 2022

Study Record Updates

Last Update Posted (ACTUAL)

July 28, 2022

Last Update Submitted That Met QC Criteria

July 26, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • ISZU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

mandala painting 4 week

IPD Sharing Time Frame

mayıs 2022-haziran 2022

IPD Sharing Access Criteria

emity

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

Drug and device information, study documents

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

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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