The Effect of Conscious Awareness Development Psychoeducation Program Prepared for Caregivers

NCT ID: NCT06675773

Last Updated: 2024-11-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-12-15

Study Completion Date

2025-11-15

Brief Summary

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

Detailed Description

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This study was planned in an experimental design with pre-test post-test follow-up measurements, experimental and control groups. The universe of the study consisted of care personnel working in institutions affiliated to the Provincial Directorate of Family, Labor and Social Services located in a city center in the east of Turkey. The sample calculation was made using the G-Power program (Experiment 14, Control 14). Since there may be omissions, the experimental group was determined as 20 participants and the control group as 20 participants. In this study, a nine-session training program will be applied to the experimental group. No application will be made to the control group. The conscious awareness development psychoeducation program will be applied once a week and for 90 minutes. Each session will be conducted in line with certain objectives. The sessions will be conducted by the investigator. Ethics committee approval was obtained before starting the study. Institutional permissions and written informed consent will be obtained for the participants. Informed consent will include information about the research and information that will ensure confidentiality.

Conditions

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Mental Health Issue

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups were mindfulness-based psychoeducation controls.
Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Investigators
The training will be conducted by the investigator. The experimental and control groups will be assigned by a statistics expert other than the investigators.

Study Groups

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Experimental Group

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.

Group Type EXPERIMENTAL

Conscious Awareness Development Psychoeducation Program

Intervention Type OTHER

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.

Control Group

No application will be made to the Control Group.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Conscious Awareness Development Psychoeducation Program

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.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* 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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Kafkas University

OTHER

Sponsor Role lead

Responsible Party

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Nilüfer KIRANŞAL

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nilüfer KIRANŞAL

Role: PRINCIPAL_INVESTIGATOR

Lecturer

Locations

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Faculty of Health Sciences Kafkas University

Kars, Merkez, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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Nilüfer KIRANŞAL

Role: CONTACT

+905053573304

Fadime KAYA SOYLU

Role: CONTACT

+905353923057

Facility Contacts

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Nilüfer KIRANŞAL, Lecturer

Role: primary

+905053573304

Related Links

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Other Identifiers

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KAÜ-SBF-NK 01

Identifier Type: -

Identifier Source: org_study_id

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