- Design
- Pre-registered systematic review and meta-analysis of randomised trials, GRADE-rated
- Population
- 16 trials, 1,992 participants receiving long-term psychodynamic psychotherapy for depression
- Primary outcome
- Reduction in depressive symptoms at end of treatment
- Effect
- Standardised mean difference 0.34 (0.20 to 0.47) vs all comparators, high-certainty; 0.27 vs active treatments, moderate-certainty
A pre-registered GRADE meta-analysis pooled 16 randomised trials and 1,992 participants of long-term psychodynamic psychotherapy — defined as at least nine months and 30 sessions — for depression. At the end of treatment it reduced depressive symptoms against all comparators (standardised mean difference 0.34, 95% CI 0.20 to 0.47), with effects generally sustained at follow-up.
The certainty is the notable part. GRADE rated the all-comparators result as high-certainty, and the comparison against active treatments as moderate-certainty (standardised mean difference 0.27). The larger effect seen against active controls specifically was very-low certainty, and risk of bias was a concern in most trials, so the firm claim is the modest one.
For practice, this supports offering or referring for long-term psychodynamic therapy as a real option in suitable patients with depression, particularly where shorter or pharmacological approaches have not held. It does not displace first-line treatments, but it gives the longer psychotherapy a firmer evidence base than it has usually been granted.
- Sixteen randomised trials, 1,992 participants; therapy of at least nine months and 30 sessions.
- Reduced depressive symptoms versus all comparators: standardised mean difference 0.34 (95% CI 0.20 to 0.47), high-certainty.
- Versus active treatments: standardised mean difference 0.27 (0.1 to 0.45), moderate-certainty.
- Effects were generally sustained at follow-up.
- Consider it for suitable patients, especially where shorter or drug approaches have not held.
Why it matters
Long psychodynamic therapy is often treated as poorly evidenced; a high-certainty synthesis gives it a firmer footing in the treatment conversation.
Don't overread it
The high-certainty finding is for a modest effect against all comparators; the larger advantage over active treatments was very-low certainty.
The statistics, in plain English
A standardised mean difference of about 0.3 is a small-to-moderate benefit; high-certainty means further research is unlikely to overturn it, while the larger effect against active controls is very-low certainty and should not be relied on.
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