study of The effect non-pharmacological Palliative Method on severity of pain and the rate of referral to the clinic in Adolescences with sickle cell
Not Applicable
- Conditions
- Sickle Cell Anemia.Sickle-cell disorders
- Registration Number
- IRCT20180128038531N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Non-acute and chronic physical and mental illness
Not having mental-emotional disturbances
A history of frequent visits to the clinic or admission to the hospital due to pain (at least once a year)
Failure to receive Pain Care Education in advance
Use only oral hygiene drugs such as acetaminophen or profen.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain severity. Timepoint: 4 Weeks before Training. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Reduce referring. Timepoint: 4 and 8 weeks after training. Method of measurement: Patient report.