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