Evaluation of the effectiveness of spiritual intervention on pain intensity and quality of life in end-of-life patients
Not Applicable
Recruiting
- Conditions
- Reducing pain and quality of life.
- Registration Number
- IRCT20210513051282N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
According to medical parameters, they are less than 6 months old
Has at least a diploma
Age 19 years and above
Believes in the Shia religion
Awareness above 8
Exclusion Criteria
Decrease the patient's level of consciousness to less than 8 during interventions for 4 consecutive days
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduce pain. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Von Korf Pain Intensity Questionnaire.;Quality of Life. Timepoint: Von Korf Pain Intensity Questionnaire. Method of measurement: Quality of Life Questionnaire.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What neurobiological pathways link spiritual interventions to pain modulation in terminal cancer patients?
How does spiritual intervention compare to opioid-based analgesia in end-stage palliative care outcomes?
Are there biomarkers like cortisol or cytokine levels predicting spiritual intervention efficacy in hospice populations?
What adverse events are associated with spiritually guided pain management in advanced disease stages?
What combination therapies integrate spiritual practices with pharmacological approaches for end-of-life symptom control?