Psychoeducation for caregivers of cancer patients using positive psychotherapy
The Effect of Positive Psychotherapy Balance Model Based Psychoeducation on Balanced Life, Psychological Well-Being and Self-Efficacy in Caregivers of Oncology Patients.
This study tests a new support program for caregivers of cancer patients to see if it helps them feel better and manage their own lives while caring for others.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization Academic / other |
| Locations | 1 site (Kağithane, İ̇stanbul) |
| Trial ID | NCT06498258 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of a psychoeducation intervention based on the positive psychotherapy balance model for individuals caring for oncology patients. It employs a randomized control group design with pretest and posttest assessments to evaluate changes in balanced life, psychological well-being, and self-efficacy among caregivers. The study aims to address the challenges faced by caregivers, who often struggle to balance their caregiving responsibilities with their personal needs. By focusing on the psychological aspects of caregiving, the intervention seeks to enhance the overall quality of life for these individuals.
Who should consider this trial
Good fit: Ideal candidates for this study are caregivers aged 18 and above who are involved in the care of oncology patients and reside in Istanbul.
Not a fit: Patients who have psychiatric illnesses or communication disabilities may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the psychological well-being and life balance of caregivers, leading to better care for oncology patients.
How similar studies have performed: Other studies have shown positive outcomes with psychoeducation interventions for caregivers, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * To be in the age group of 18 and above * To have a score of 90 and below on the Barthel VAS Index * To be at least primary school graduate * To have no psychiatric illness (diagnosis) * To have no communication and comprehension disability related to vision, hearing * To live in Istanbul Exclusion Criteria: * Not having attended all sessions of the training programme * Not having answered any of the pre-test, post-test and follow-up tests
Where this trial is running
Kağithane, İ̇stanbul
- Prof. Dr. Cemil Taşcıoğlu City Hospital — Kağithane, İ̇stanbul, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Servet Cihan — Prof. Dr. Cemil Taşcıoğlu Şehir Hastanesi
- Study coordinator: Servet Cihan, Education nurse
- Email: servetcihann@hotmail.com
- Phone: 5456925693
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.