| Adverse events | Total adverse events did not differ significantly between Rhodiola rosea and placebo groups by day 42.No clear benefit | Not reported Recorded unit: Not reported | Sample (as reported): 48 Follow-up: day 42 | Randomised trial · 2014 Study detailsRhodiola rosea for mental and physical fatigue in nursing students: a randomized controlled trial. Randomized Controlled Trial PMID 25268730 |
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| Fatigue (VAS-F) at day 42 | Rhodiola rosea worsened VAS-F fatigue scores by 1.9 versus placebo at day 42 (p=0.015). (95% CI 0.4, 3.5; p = 0.015)Possible harm | 1.9 Recorded unit: Not reported | Sample (as reported): 48 Follow-up: day 42 | Randomised trial · 2014 Study detailsRhodiola rosea for mental and physical fatigue in nursing students: a randomized controlled trial. Randomized Controlled Trial PMID 25268730 |
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| Vitality subscale (RAND-36) at day 42 | Rhodiola rosea worsened vitality scores by -17.3 versus placebo at day 42 (p=0.011). (95% CI -30.6, -3.9; p = 0.011)Possible harm | -17.3 Recorded unit: Not reported | Sample (as reported): 48 Follow-up: day 42 | Randomised trial · 2014 Study detailsRhodiola rosea for mental and physical fatigue in nursing students: a randomized controlled trial. Randomized Controlled Trial PMID 25268730 |
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| attention (CCPT II indices: omissions, Hit RT SE, variability) | Rhodiola rosea (SHR-5) significantly improved attention test indices compared with placebo over 28 days (n=60).Benefit seen | Not reported Recorded unit: Not reported | Sample (as reported): 60 Follow-up: 28 days | Randomised trial · 2009 Study detailsA randomised, double-blind, placebo-controlled, parallel-group study of the standardised extract shr-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Randomized Controlled Trial PMID 19016404 |
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| burnout symptoms (Pines' burnout scale) | Rhodiola rosea (SHR-5) significantly improved burnout symptoms compared with placebo over 28 days in fatigue syndrome patients (n=60).Benefit seen | Not reported Recorded unit: Not reported | Sample (as reported): 60 Follow-up: 28 days | Randomised trial · 2009 Study detailsA randomised, double-blind, placebo-controlled, parallel-group study of the standardised extract shr-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Randomized Controlled Trial PMID 19016404 |
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| cortisol response to awakening stress | Rhodiola rosea (SHR-5) significantly decreased cortisol response to awakening stress compared with the placebo (control) group over 28 days (n=60).Benefit seen | Not reported Recorded unit: Not reported | Sample (as reported): 60 Follow-up: 28 days | Randomised trial · 2009 Study detailsA randomised, double-blind, placebo-controlled, parallel-group study of the standardised extract shr-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Randomized Controlled Trial PMID 19016404 |
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| mental health (SF-36) and depression (MADRS) | Mental health (SF-36) and depression (MADRS) scores improved similarly in both Rhodiola and placebo groups, a placebo effect (n=60).No clear benefit | Not reported Recorded unit: Not reported | Sample (as reported): 60 Follow-up: 28 days | Randomised trial · 2009 Study detailsA randomised, double-blind, placebo-controlled, parallel-group study of the standardised extract shr-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Randomized Controlled Trial PMID 19016404 |
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| Mental performance / Fatigue Index tests after night duty | RRE significantly improved mental performance test scores compared with placebo during two-week treatment periods.Benefit seen | Not reported Recorded unit: Not reported | Sample (as reported): 56 Follow-up: two weeks | Randomised trial · 2000 Study detailsRhodiola rosea in stress induced fatigue--a double blind cross-over study of a standardized extract SHR-5 with a repeated low-dose regimen on the mental performance of healthy physicians during night duty. Randomized Controlled Trial PMID 11081987 |
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