NCT06675773

Brief Summary

This study aimed to increase the conscious awareness of caregivers and reduce work stress and compassion fatigue.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 4, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 5, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

December 15, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 15, 2025

Completed
Last Updated

November 13, 2024

Status Verified

November 1, 2024

Enrollment Period

11 months

First QC Date

November 4, 2024

Last Update Submit

November 11, 2024

Conditions

Keywords

Mindfulness,Work stressCompassion FatiguePsychoeducation

Outcome Measures

Primary Outcomes (1)

  • The Mindful Attention Awareness Scale-MAAS

    Originally named The Mindful Attention Awareness Scale-MAAS, it measures the attention and present time awareness of an individual in their daily lives. It consists of 15 items and a single sub-dimension. The scale is in the form of a 6-point Likert and is evaluated as a single total score. Individuals who score high on the scale show that their conscious awareness levels are high (Brown and Rayn 2003, Özyeşil et al. 2011)

    Pre-test -Post-test (9 weeks) Follow-up ( 3 month after)

Secondary Outcomes (2)

  • General Work Stress Scale

    Pre-test -Post-test (9 weeks) Follow-up ( 3 month after)

  • Compassion Fatigue Scale- Short Scale Form

    Pre-test -Post-test (9 weeks) Follow-up ( 3 month after)

Study Arms (2)

Experimental Group

EXPERIMENTAL

The Conscious Awareness Development Psychoeducation Program will be applied to the experimental group. Conscious awareness and self-compassion techniques will be used in the psychoeducation program sessions. Homework will be given to the participants in each session. The psychoeducation program is prepared based on conscious awareness.

Other: Conscious Awareness Development Psychoeducation Program

Control Group

NO INTERVENTION

No application will be made to the Control Group.

Interventions

The Conscious Awareness Development Psychoeducation Program consists of nine sessions. The sessions will be applied once a week and last 90 minutes. The psychoeducation program is prepared based on conscious awareness. Conscious awareness and self-compassion techniques will be used in the sessions. Homework will be given to the participants in each session.

Experimental Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being over 18 years of age,
  • Being actively working as a care worker in relevant institutions.

You may not qualify if:

  • Having received similar training before
  • Having been diagnosed with a mental illness
  • Wanting to leave the study at any stage.
  • Not having attended more than two sessions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Health Sciences Kafkas University

Kars, Merkez, 36100, Turkey (Türkiye)

Location

Related Links

MeSH Terms

Conditions

Occupational StressCompassion Fatigue

Condition Hierarchy (Ancestors)

Occupational DiseasesStress, PsychologicalBehavioral SymptomsBehaviorMental FatigueFatigueSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Nilüfer KIRANŞAL

    Lecturer

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Nilüfer KIRANŞAL

CONTACT

Fadime KAYA SOYLU

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Masking Details
The training will be conducted by the investigator. The experimental and control groups will be assigned by a statistics expert other than the investigators.
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Two groups were mindfulness-based psychoeducation controls.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

November 4, 2024

First Posted

November 5, 2024

Study Start

December 15, 2024

Primary Completion

November 15, 2025

Study Completion

November 15, 2025

Last Updated

November 13, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Locations