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Bio-AnalystSupplement research
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Rhodiola

Selected research topic

Stress and mood

The confirmed comparison studies tested several ingredients together. They cannot isolate the effect of this ingredient.

Some findings concern patients or people with a deficiency.

Publications for this topic
8
Human comparison publications
1
Publications needing review
5

Findings in the studies

  • Outcome needs clarification

    Publications linked to this measurement: 1

    About this measure

    Original outcome name: SDS

    • Results were mixed for this outcome.

      Several ingredients were tested together, so this ingredient’s individual effect is unknown.

      Patient group · Combination study · 3 months
      Measurement and study conditions
      Study type
      Randomized controlled trial: subjects were randomly assigned to groups for comparison.
      Study population
      Human participants · Patient group
      Ingredients tested
      Ingredient combination
      How results were compared
      Results were compared between groups. · Study comparison: overall three-arm comparison null, while reported pairwise/post-treatment directions conflict
      Measurement time
      3 months
  • Anxiety symptom score

    Publications linked to this measurement: 1

    About this measure

    mean HARS scores

    Other human research, including observational studies and reviews
    • A change was reported before and after use. Its cause cannot be isolated.
      Patient group · Single ingredient · 10 weeks
      Measurement and study conditions
      Study type
      Clinical trial
      Study population
      Human participants · Patient group
      Ingredients tested
      Single ingredient
      How results were compared
      Changes within the same group were compared. · Study comparison: Within-person HARS change after Rhodiola treatment
      Additional measurement information
      Secondary outcome
      Measurement time
      10 weeks
  • stress symptoms

    Publications linked to this measurement: 1

    Other human research, including observational studies and reviews
    • A change was reported before and after use. Its cause cannot be isolated.
      Patient group · Single ingredient · 3 days, 1 week, and 4 weeks
      Measurement and study conditions
      Study type
      Clinical trial
      Study population
      Human participants · Patient group
      Ingredients tested
      Single ingredient
      How results were compared
      Changes within the same group were compared. · Study comparison: within-group questionnaire changes; nonrandomized open-label single-arm with no concurrent control
      Additional measurement information
      Secondary outcome
      Measurement time
      3 days, 1 week, and 4 weeks

This result is held for interpretation. That does not mean research found no effect.

Outcome groups needing additional review (2)
  • Depression symptom score · Distinct papers needing additional review: 1Evidence criteria check: 1
  • situational anxiety · Distinct papers needing additional review: 1Direction unclear: 1

One paper can appear under multiple measured outcomes or review reasons, so these counts should not be added together.

Representative outcome and study details

Human studies reported a within-group change in mean HARS scores.

Single-ingredient studies · Human studies · Includes patient groups · within-group comparison

1 publications linked to this result

  • Route, form, dose, or population details are incomplete, so the findings cannot be confirmed as directly comparable.
Data coverage and detailed study classifications

Paper counts are separated by research topic below. One paper may contribute to multiple findings.

Analysis status: Public-ready

Ingredient analysis date:

How the grade was determined: B

The 60.9 evidence score includes 8 independent human studies and 8 clinical studies in the representative benefit area. The B tier remains conservative because of limited repetition across independent human clinical studies.

The grade is based mainly on the research area with the most evidence. It does not mean the same result was found in other areas.

Papers linked to this ingredient overall: 92

Papers linked to this topic 8 · distinct papers 8 · papers with a confirmed human comparison 1 · papers needing additional review 5

A publication may appear in more than one count. These numbers should not be added. Ingredient-wide papers, topic-linked papers, and sources in outcome groups use different scopes. Adding source counts may count the same paper more than once.

  • Depression symptom score (HAM-D): Sources represented in this measurement group: 1 · Distinct papers with human comparisons for this outcome: 0
  • Anxiety symptom score (mean HARS scores): Sources represented in this measurement group: 1 · Distinct papers with human comparisons for this outcome: 0
  • SDS: Sources represented in this measurement group: 1 · Distinct papers with human comparisons for this outcome: 1
  • situational anxiety: Sources represented in this measurement group: 1 · Distinct papers with human comparisons for this outcome: 0
  • stress symptoms: Sources represented in this measurement group: 1 · Distinct papers with human comparisons for this outcome: 0

What the research found

SDS

Results for this measurement were mixed; no consistent conclusion can be drawn.

Controlled study in people · Ingredient combination · Patient group

Several ingredients were used together. This does not establish the effect of this ingredient alone or synergy.

Between-group comparison

Analysis coverage and paper counts

1 paper · 1 measured outcome

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

mean HARS scores

A change was reported before and after use. Its cause cannot be isolated.

Other evidence · Single ingredient · Patient group

Within-group comparison

Analysis coverage and paper counts

1 paper · 1 measured outcome

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

stress symptoms

A change was reported before and after use. Its cause cannot be isolated.

Other evidence · Single ingredient · Patient group

Within-group comparison

Analysis coverage and paper counts

1 paper · 1 measured outcome

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

HAM-D

The study needs further checking before its result can be interpreted.

Controlled study in people · Single ingredient · Patient group

Between-group comparison

Analysis coverage and paper counts

1 paper · 1 measured outcome

1 papers held from direction counts

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

situational anxiety

The study needs further checking before its result can be interpreted.

Other evidence · Ingredient combination · General population

Several ingredients were used together. This does not establish the effect of this ingredient alone or synergy.

The comparison could not be confirmed.

Analysis coverage and paper counts

1 paper · 1 measured outcome

1 papers held from direction counts

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

Unspecified measured outcome

The study needs further checking before its result can be interpreted.

Review · Ingredient combination · Unspecified population

Several ingredients were used together. This does not establish the effect of this ingredient alone or synergy.

The comparison could not be confirmed.

Analysis coverage and paper counts

1 paper · 1 measured outcome

1 papers held from direction counts

Review overlap with primary papers is unknown; counts stay separate.

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

Unspecified measured outcome

The study needs further checking before its result can be interpreted.

Controlled study in people · Single ingredient · Patient group

Between-group comparison

Analysis coverage and paper counts

1 paper · 1 measured outcome

1 papers held from direction counts

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

Unspecified measured outcome

The study needs further checking before its result can be interpreted.

Controlled study in people · Single ingredient · Unspecified population

The comparison could not be confirmed.

Analysis coverage and paper counts

1 paper · 1 measured outcome

1 papers held from direction counts

Direction counts are distinct papers within each row. Outcome contributions count endpoint results, so one paper may contribute more than once.

How to read research findings

How should I read research findings?

Research guides

Side effects and combination findings

Findings from this ingredient alone are shown separately from those involving another supplement or medication.

No reviewed caution rules are available yet. Reported caution findings are shown below.

Review 1 combination findings and 0 findings that outperformed an ingredient alone.

Findings to review with care

Side effects reported for the ingredient alone are separated from findings involving another supplement or medication.

Cautions reported with another supplement or medication

These studies reported worsening outcomes, reduced absorption, or other cautions with combined use. They do not predict an individual's outcome.

SSRIsPotential risk of serotonin syndrome when combined with SSRIs.
Tricyclic antidepressantsPotential risk of serotonin syndrome when combined with tricyclic antidepressants.

Reported improvements with combinations

Combination findings are grouped by how the study compared them. This is not a recommendation to combine ingredients.

Combinations with reported improvement

The combination showed improvement, but each ingredient's contribution is unclear.

CaffeineA randomized, double-blind, placebo-controlled trial in 48 male volleyball players found that combined Rhodiola rosea and caffeine supplementation significantly improved jump height, reduced power decline during high-frequency jumps, and lowered perceived exertion compared to placebo and single-agent groups.