- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06339762
Self-Compassion Training Given to Relatives of Patients in Palliative Care
June 7, 2024 updated by: Gülcan Bahçecioğlu Turan, Firat University
''Invitation to Self-Compassion: Reshaping the Burden of Care in the Light of Self-Compassion Training Given to Relatives of Patients in Palliative Care.''
The concept of self-compassion is a concept that has been frequently the subject of research lately and has gained importance along with positive psychology.
It is also referred to as self-understanding and self-compassion in the literature.
The concept of self-compassion used in our study represents the concept of self-compassion in its original form as used in foreign sources.
Compassion is classified according to the source to which it is directed or received.
It is suggested that there are three different flows: the feeling of compassion that the individual directs from himself to others, the feeling of compassion he receives from others, and the feeling of compassion that he directs directly to his own self.
It means showing oneself the same compassion and understanding one does to others, accepting and being open to one's own pain, and being accepting of oneself without being judgmental.
Individuals with self-compassion believe that the difficulties, flaws and shortcomings they experience are normal.
At the same time, they are aware that being human has characteristics and that everyone can experience these situations.
Individuals may be less compassionate towards themselves than they are towards others.
Individuals with self-compassion are as understanding, forgiving and loving towards themselves as they are towards other people.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
Center
-
Elazığ, Center, Turkey, 25240
- Fırat university
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being an inpatient in the Palliative unit of Erzurum City Center City Hospital
- Not having attended self-compassion training before
- The patient's relatives do not have any obstacle to communication
- Participants who gave informed consent to participate in the study.
Exclusion Criteria:
- Relatives of patients who do not agree to participate in the research,
- The participant must have attended self-compassion training before,
- People have a condition that prevents communication
- The occurrence of a physical or psychological problem in people during the research process
- Patient's relatives want to leave before completing the training
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental
Self-Compassion Training
|
Self-Compassion Training
|
|
No Intervention: Control
Self-Compassion Training no
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-Compassion Scale:
Time Frame: 4 week
|
Self-compassion is the individual's ability to show the same compassion to himself as he does to others.
The scale, whose original name was "self-compassion scale", was developed by Neff (2003b).
The purpose of the scale is to measure individuals' self-compassion levels, that is, their self-compassion levels.
The scale consists of 26 items and the questions are evaluated on a 5-point Likert scale.
The scale has 6 sub-dimensions: self-compassion, self-judgment, common human experiences, conscious awareness, isolation and over-identification.
Cronbach's alpha values of the subscales vary between .78 and .81,
and the Cronbach's alpha value of the entire scale is .92.
|
4 week
|
|
Care Burden Scale:
Time Frame: 4 week
|
It was developed by Zarit, Reever and Bach-Peterson in 1980.
In studies, the internal consistency coefficient of the scale was found to be between 0.87 and 0.94, and the test-retest reliability was found to be 0.71 (Zarit, 1990).
Turkish validity and reliability study was conducted by İnci and Erdem (2008), and the Cronbach alpha reliability coefficient was found to be 0.95.
It is a scale used to evaluate the stress experienced by caregivers of individuals or elderly people in need of care.
|
4 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
February 13, 2024
Primary Completion (Actual)
March 13, 2024
Study Completion (Actual)
June 8, 2024
Study Registration Dates
First Submitted
February 23, 2024
First Submitted That Met QC Criteria
March 27, 2024
First Posted (Actual)
April 1, 2024
Study Record Updates
Last Update Posted (Actual)
June 11, 2024
Last Update Submitted That Met QC Criteria
June 7, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2024/03-19
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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