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Logotherapy Counseling Programme for Palliative Care Patients With Chronic Sorrow

B

Baskent University

Status

Enrolling

Conditions

Cancer
Palliative Care

Treatments

Other: Logotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05129059
KA21/276

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness of logotherapy counseling program on chronic sorrow, meaning of life and dignity of palliative care patients.

Full 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.

Enrollment

58 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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%

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

58 participants in 2 patient groups

Logotherapy
Experimental group
Description:
Participants will receive individual logotherapy counseling by the investigator for 8 visits in 4 weeks.
Treatment:
Other: Logotherapy
Control
No Intervention group
Description:
Participants will receive routine care.

Trial contacts and locations

1

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Central trial contact

Yasemin Eskigülek

Data sourced from clinicaltrials.gov

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