Effectiveness of Laying-on-of-hands for Sickle Cell Disease
1 other identifier
interventional
40
1 country
1
Brief Summary
The objective of this study is to evaluate the effectiveness of 1-year administration of laying-on-of-hands on the morbidity and mortality of patients with sickle cell disease in Africa.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_2
Started Mar 2006
Typical duration for phase_2
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2009
CompletedFirst Submitted
Initial submission to the registry
January 21, 2012
CompletedFirst Posted
Study publicly available on registry
January 25, 2012
CompletedApril 13, 2015
January 1, 2012
1 year
January 21, 2012
April 9, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
disease-related episodes and mortality
3 years and 9 months
Secondary Outcomes (1)
blood data
1 year
Study Arms (2)
laying-on-of-hands
EXPERIMENTALPatients of this arm received laying-on-of-hands twice a day (45 minutes each) every weekday for 1year, and received conventional medical treatment if necessary.
control group
NO INTERVENTIONPatients of this arm did not receive any alternatives other than conventional treatment.
Interventions
The intervention group received laying-on-of-hands every weekday for 1 year along with conventional medicine. The control group did not undergo any alternatives to OPT.
Eligibility Criteria
You may qualify if:
- patients with symptoms associated with sickle cell disease
- those able to receive laying-on-of-hands every weekday for 1 year
- those able to receive conventional medical treatment whenever necessary
- those able to receive blood test at the beginning, after 6 month and after 1 year
You may not qualify if:
- those who wish to use other complementary and alternative therapies along with laying-on-of-hands
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The national medical center for sickle cell disease
Kinshasa, Democratic Republic of the Congo
Related Publications (1)
Minga TM, Koto FK, Egboki H, Suzuki K. Effectiveness of biofield therapy for individuals with sickle cell disease in Africa. Altern Ther Health Med. 2014 Jan-Feb;20(1):20-6.
PMID: 24445353DERIVED
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Kodondi K Koto, MD, PhD
The Institute of Scientific Research for Health, Kinshasa
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- president
Study Record Dates
First Submitted
January 21, 2012
First Posted
January 25, 2012
Study Start
March 1, 2006
Primary Completion
March 1, 2007
Study Completion
December 1, 2009
Last Updated
April 13, 2015
Record last verified: 2012-01