REF-1656 · Yun et al., 2026 · International Journal of Clinical Pharmacy, · Paper · PubMed

Short-term antidepressant use made exercise feel slightly harder without consistently lowering performance: in 10 crossover trials of 99 male athletes, RPE rose 0.52 points on the Borg 6-20 scale while time trial, power, heart rate and lactate showed no significant overall change, but reboxetine alone slowed the time trial by 3.62 min and cut mean power by 19.97 W

Main caveat: Men only and acute or short exposure, as the authors state.
moderate evidenceMeasured on recreational to highly trained athletesRead from the abstract only

Yun and colleagues asked whether taking an antidepressant changes objective performance and perceived exertion in athletes.

They searched SPORTDiscus, PubMed, Web of Science and the Cochrane Library up to March 2025 for randomised trials in elite, competitive or recreational athletes that compared an antidepressant with placebo or no treatment, and pooled them with random-effects models. Ten crossover trials with 99 male athletes qualified.

The drugs were reboxetine (a noradrenaline reuptake inhibitor), bupropion (a noradrenaline-dopamine reuptake inhibitor) and the SSRIs fluoxetine and paroxetine. Taken short term, the drugs raised rating of perceived exertion by 0.52 points on the 6-20 Borg scale. Time-trial performance, mean power output, heart rate and blood lactate showed no significant overall change.

In subgroups, reboxetine slowed time-trial performance by 3.62 min and lowered mean power by 19.97 W. The authors conclude that short-term use brought a small rise in perceived exertion without a consistent loss of objective performance, and that the evidence, all from men and acute dosing, says nothing yet about women or long-term treatment of athletes with depression.

Participants

99 male athletes across 10 crossover trials; inclusion allowed elite, competitive or recreational athletes.
Sports, ages, fitness, doses and timing: not in the abstract.
Whether any participant had a depressive disorder: not stated; the authors' call for studies in athletes with depressive disorders implies the trials were in athletes without one (our reading).

Methods

Search: SPORTDiscus, PubMed, Web of Science and the Cochrane Library, up to March 2025; English-language RCTs; registered in PROSPERO (CRD420251123740).
Inclusion: athletes of any level; an antidepressant against placebo or no treatment; at least one performance-related outcome, objective or subjective.
Studies: 10 crossover RCTs, 99 men.
Analysis: random-effects pooled mean differences with 95% CIs; subgroups by drug.
Quality assessment: not reported in the abstract.

Key Results

OutcomeAntidepressant vs control
RPE (Borg 6-20)+0.52 points (95% CI 0.01-1.04; p < 0.05)
Time-trial performanceno significant overall effect
Mean power outputno significant overall effect
Heart rateno significant overall effect
Blood lactateno significant overall effect
Reboxetine subgroup: time trial3.62 min slower (95% CI 0.18-7.06; p < 0.05)
Reboxetine subgroup: mean power−19.97 W (−36.87 to −3.06), p < 0.05
The pooled confidence intervals for the null outcomes are not in the abstract.

Practical Application

On a short course of one of these drugs, expect sessions to feel a little harder rather than to go measurably slower. RPE rose about half a point on the 6-20 scale, while time-trial result, power, heart rate and lactate showed no significant overall change; a small rise in RPE at the usual power may be the drug, not fatigue.
Reboxetine was the exception. In its subgroup the time trial was 3.62 min slower and mean power 19.97 W lower; the drug class matters, so the pooled "no change" does not cover every antidepressant.
Inference, not tested here: heart rate showed no significant overall change, so heart-rate zones may need no correction for these drugs; that rests on short exposures in men, and the pooled interval for heart rate is not in the abstract.
The prescriber decides. Starting, stopping, switching or dosing an antidepressant is for the prescribing doctor; the assistant does not change medication or suggest stopping it for training. A side effect that limits training is something to take to the prescriber.
Not settled by this design: long-term treatment, athletes with depression, women, antidepressants other than reboxetine, bupropion, fluoxetine and paroxetine, and training adaptation over weeks.

Limitations

Men only and acute or short exposure, as the authors state.
10 small crossover trials; risk of bias and certainty are not in the abstract.
Drugs from different classes (a noradrenaline reuptake inhibitor, a noradrenaline-dopamine reuptake inhibitor and SSRIs) were pooled; the reboxetine subgroup shows that pooling can hide drug-specific effects.
No significant overall change is not the same as no change; the intervals for those outcomes are not in the abstract.
Written from the abstract and the PubMed record; full text not read.
How this entry was checked and changed
Why this level

risk of bias not read (abstract only): the abstract reports no risk-of-bias or certainty result; 10 small crossover trials with 99 men in all and acute exposure

Content correction 2026-11-07
2026-11-07: added from the abstract and the PubMed record; level B+ (meta-analysis of 10 crossover trials, risk of bias not read).