Clinical trial of Rhodiola rosea L. extract SHR-5 in the treatment of mild to moderate depression
Darbinyan V, Aslanyan G, Amroyan E, Gabrielyan E, Malmstrom C, Panossian A
Published in Nordic Journal of Psychiatry, Vol. 61, pp. 343-348
Methodology
Randomised, double-blind, placebo-controlled parallel-group phase III trial over 6 weeks; 89 patients with DSM-IV mild-to-moderate depression received SHR-5 at 340 mg/day, 680 mg/day, or placebo.
Key Findings
Both active groups improved significantly in overall depression, insomnia, emotional instability and somatisation compared with baseline, while the placebo group showed no significant improvement; self-esteem did not improve.
Conclusions
Standardised SHR-5 extract showed antidepressant activity in mild to moderate depression with no serious side effects reported.
Limitations
Single-country trial, six-week duration, manufacturer-affiliated authorship, no active comparator.
Supplements Studied
For individuals in groups A and B, overall depression, together with insomnia, emotional instability and somatization, but not self-esteem, improved significantly following medication, whilst the placebo group showed no improvement.
Outcomes Measured
Overall depression, together with insomnia, emotional instability and somatization, but not self-esteem, improved significantly following medication, whilst the placebo group showed no improvement.
Rhodiola improved overall depression, insomnia and emotional instability scores versus placebo
Rhodiola improved overall depression, insomnia and emotional instability scores versus placebo
Related Health Concerns
Study Details
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Disclosures
Funding
Swedish Herbal Institute (extract manufacturer)
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