Clinical trial · Observational
Spirituality/Religiosity in Patients and Caregivers
A Preliminary Study of Spirituality/Religiosity, Symptom Distress and Quality of Life Among Palliative Care Patients and Their Primary Caregivers
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Primary Objective: -To examine the association between self-rated spirituality/religiosity and coping strategies (Brief RCOPE, Brief COPE, SBI-15R) among palliative care patients. Secondary Objectives: * To examine the associations between self-rated spirituality/religiosity and physical (ESAS) and psychological symptom reports (HADS), and quality of life (FACIT-sp) among palliative care patients. * To examine the association between patient's self-reported spirituality/religiosity, and primary caregiver distress (HADS, PSQI, CQLS-C, caregiver self-assessment questionnaire, FACIT-sp). * To determine the frequency (self-rated spiritual pain scale when score is more or equal than 1 in the scale 0 to 10) and intensity of self-rated spiritual pain in the palliative care setting and to explore the association between spiritual pain, and negative religious coping (Brief RCOPE), physical (ESAS) and psychological symptoms (HADS), and primary caregiver distress (CQLS-C, caregiver self-assessment questionnaire). * To examine the association between primary caregivers' spirituality/religiosity (Appendix H, first question), religious coping strategies (Brief-RCOPE) and psychological and family/caregiver distress (HADS, PSQI, CQLS-C, caregiver self-assessment questionnaire), and caregivers' spiritual pain (Appendix F, second question).
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Advanced Cancer | Malignant Neoplasm | CURATED_BROADER | 0.78 |
| Solid Tumors | Solid Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Questionnaires | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Patients
- description
- Patients with advanced cancer receiving palliative care.
- interventionNames
- Behavioral: Questionnaires
- label
- Caregivers
- description
- Primary caregivers of Patients with advanced cancer receiving palliative care.
- interventionNames
- Behavioral: Questionnaires
Primary outcomes (1)
- measure
- Association between self-rated spirituality/religiosity and coping strategies
- timeFrame
- Questionnaires completed by patient/caregiver at second consult visit, estimate 40 minutes to finish forms.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. (Patients) Advanced cancer patients seen in palliative care outpatient clinic and palliative care mobile team and inpatient unit at M.D. Anderson Cancer Center 2. (Patients) Patients aged 18 years or over 3. (Patients) Karnofsky performance status score of more than 40 at time of inclusion into study. (Patients with Karnofsky score less than 40 may not be able to complete the measures). 4. (Patients) Able to provide informed consent and comply with study procedures 5. (Caregivers) Spouse, first degree relative, or other person designated by the patient as providing direct assistance to the patient in his/her activities of daily living 6. (Caregivers) Having the patient's consent to be contacted. 7. (Caregivers) Caregiver is 18 years or over 8. (Caregivers) Able to provide informed consent and comply with study procedures 9. (Patients) only English-speaking, as determined by their ability to understand the informed consent and the assessment tools. 10. (Caregivers) only English-speaking, as determined by their ability to understand the informed consent and the assessment tools. 11. (Patients) Normal cognitive status as determined by the interviewer based on the ability to understand the nature of the study and consent process. Exclusion Criteria: N/A
References
Publications (0)
Data not yet available