To assess the two components of individualized homeopathic treatment for acute depression, i.e., to investigate the specific effect of individualized Q-potencies versus placebo and to investigate the effect of different approaches to the homeopathic case history taking(defined in this study as case history taking type I and II).
Homeopathy is often sought by patients with depression. In classical homeopathy, the treatment consists of two main elements: the taking of the case history and the prescription of an individually selected homeopathic remedy. Homeopathic medicines are produced through sequential, agitated dilutions. A Q-Potency is prepared by grinding the raw material, followed by a process of consecutive 1:50.000 agitated dilutions. Previous data suggest that individualized homeopathic Q-potencies were non inferior to the antidepressant fluoxetine in a sample of patients with moderate to severe major depression. The question remains whether individualized homeopathic Q-potencies have a specific therapeutical effect in acute depression as this has not yet been investigated.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
44
individualised homeopathic medicines
placebo
one special homeopathic technique for case history taking
Institute for Social Medicine, Epidemiology, and Health Economics, Charité University Medical Center Berlin, Germany
Berlin, State of Berlin, Germany
primary endpoint is the mean total depression score post treatment
total score on the 17-item Hamilton Depression Rating Scale - (HAM-D)
Time frame: six weeks
mean total depression score during the treatment
total score on Hamilton Depression Rating Scale (HAM-D)
Time frame: two and four weeks
response and remission rates
response (decrease of 50% or more from baseline HAM-D score); remission (HAM-D scores ≤ 7)
Time frame: two, four and six weeks
Self-rated depression score
Beck Depression inventory (BDI) total score
Time frame: two, four and six weeks
quality of life assessment
total mean score on the SF-12 Health Survey
Time frame: two, four and six weeks
Safety
Adverse events will be collected during the study and will form part of the secondary endpoint data in determining the safety of homeopathic medicines. Adverse events and serious adverse events will be registered in accordance with the ICH-Guidelines for Good Clinical Practice
Time frame: two, four and six weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
another type of homeopathic case history taking