rct
    2007

    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

    Year:2007
    Sample Size:89
    Duration:6 weeks
    Quality Score:6/10

    Disclosures

    Funding

    Swedish Herbal Institute (extract manufacturer)

    This information is for educational purposes only. Always consult a healthcare professional before starting any supplement regimen.