- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05129059
Logotherapy Counseling Programme for Palliative Care Patients With Chronic Sorrow
The Effect of Logotherapy Counseling Programme on Dignity and Chronic Sorrow in Palliative Care Patients Experiencing Chronic Sorrow
Study Overview
Detailed Description
Palliative care patients experience psychosocial and spiritual problems such as depressed mood, fear of metastasis, uncertainty, lack of pleasure, fear of suffering, and chronic sorrow. Logotherapy is a meaning-centered intervention helping the individual to discover the meaning of life and increasing the spiritual well-being and quality of life of the individual. In this study, the effect of logotherapy counseling program on dignity, chronic sorrow and meaning of life of palliative care patients will be evaluated.
In this study, the participants will be randomized in a single blind manner (participant) to either intervention (8 session-4 week logotherapy) or control (routine care) groups.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Yasemin Eskigülek
- Phone Number: +905447887405
- Email: yaseminuslu12@gmail.com
Study Locations
-
-
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Ankara, Turkey, 06560
- Recruiting
- Gazi University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Hospitalized patients due to advanced cancer Patients informed of cancer diagnosis at least 1 month Patients reporting to have chronic sorrow Patients with palliative performance scale score at least 50% Patients having life expectancy more than 6 months Patients who volunteered to participate in the study and signed written informed consent
Exclusion Criteria:
Clinically diagnosed mental disorder Patients with palliative performance scale score < 40%
Study Plan
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Logotherapy
Participants will receive individual logotherapy counseling by the investigator for 8 visits in 4 weeks.
|
Logotherapy is a method of finding meaning with three basic principles.
The first principle is that life is meaningful in every situation , even in the most desperate moments.
The second principle is that the main source of motivation is the desire to find meaning in life.
The third is that an individual is free to choose his own attitude even in the worst conditions.
|
NO_INTERVENTION: Control
Participants will receive routine care.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
meaning in life
Time Frame: baseline and 8 weeks
|
Meaning in life scale is a validated, 7-points Likert type scale with 2 dimensions.
Possible scores range from 5 to 35 for each dimensions.
Change= score of present meaning subscale> searched meaning subscale (8 week subscale-baseline subscale
|
baseline and 8 weeks
|
dignity
Time Frame: baseline and 8 weeks
|
The Patient Dignity Inventory is a valid, 5-points Likert type scale with 5 dimensions.
Possible scores range from 25-125.
Change= Lower score from the patient dignity inventory at the end of intervention compared to baseline.
|
baseline and 8 weeks
|
chronic sorrow
Time Frame: baseline and 8 weeks
|
Prolonged grief disorder scale-patient form is a valid, 5-points Likert type scale.
Possible scores range from 12 to 60. Change= Lower score from the scale at the end of intervention compared to baseline.
|
baseline and 8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yasemin Eskigülek, Baskent University
- Study Director: Sultan Kav, Baskent University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- KA21/276
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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