Data

Meta-analysis: ultra-brief treatments for depression and anxiety

Macquarie University
Madelyne Bisby (Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.25949/30548276.v1&rft.title=Meta-analysis: ultra-brief treatments for depression and anxiety&rft.identifier=10.25949/30548276.v1&rft.publisher=Macquarie University&rft.description=The files include data relating to a meta-analysis of the efficacy of ultra-brief psychological treatments for anxiety and depression. The files include (1) data relating to between-group effect sizes, (2) data relating to risk of bias ratings for included studies, and (3) data relating to within-group effect sizes. ABSTRACT FROM ASSOCIATED MANUSCRIPT:Depression and anxiety are common but most adults experiencing these symptoms do not receive psychological treatment. Ultra-brief psychological treatments are a time-limited and potentially lower cost option for those who would otherwise not receive treatment. This prospectively registered review examined the acceptability and efficacy of ultra-brief psychological treatments for adults with depression or anxiety symptoms. A systematic search was undertaken up to April 2025. All clinical trials examining an ultra-brief psychological treatment for adults with depression or anxiety symptoms were included. This review returned 16,670 results and included 34 studies (N = 3,679). High rates of uptake (91% [95% CI 86, 94]) and completion (96% [95% CI 90, 98]) were reported. Compared to control, treatment resulted in small to moderate reductions in depression g = 0.35 (k = 20, 95% CI 0.13, 0.56) and moderate reductions in anxiety g = 0.51 (k = 14, 95% CI 0.40, 0.61) at post-treatment. Within-group effects appear to be maintained at follow-up. Several moderators of between-group and within-group effects were identified. Risk of bias judgements are reported, and overall heterogeneity was high. Ultra-brief treatments appear to be acceptable and associated with significant symptom improvements. Larger clinical trials with longer follow-up periods are needed.&rft.creator=Madelyne Bisby&rft.date=2025&rft_rights= https://creativecommons.org/licenses/by/4.0/&rft_subject=Clinical psychology&rft_subject=anxiety&rft_subject=depression&rft_subject=psychology&rft_subject=ultra-brief&rft_subject=brief&rft_subject=mental health&rft.type=dataset&rft.language=English Access the data

Full description

The files include data relating to a meta-analysis of the efficacy of ultra-brief psychological treatments for anxiety and depression. The files include (1) data relating to between-group effect sizes, (2) data relating to risk of bias ratings for included studies, and (3) data relating to within-group effect sizes.

ABSTRACT FROM ASSOCIATED MANUSCRIPT:

Depression and anxiety are common but most adults experiencing these symptoms do not receive psychological treatment. Ultra-brief psychological treatments are a time-limited and potentially lower cost option for those who would otherwise not receive treatment. This prospectively registered review examined the acceptability and efficacy of ultra-brief psychological treatments for adults with depression or anxiety symptoms. A systematic search was undertaken up to April 2025. All clinical trials examining an ultra-brief psychological treatment for adults with depression or anxiety symptoms were included. This review returned 16,670 results and included 34 studies (N = 3,679). High rates of uptake (91% [95% CI 86, 94]) and completion (96% [95% CI 90, 98]) were reported. Compared to control, treatment resulted in small to moderate reductions in depression g = 0.35 (k = 20, 95% CI 0.13, 0.56) and moderate reductions in anxiety g = 0.51 (k = 14, 95% CI 0.40, 0.61) at post-treatment. Within-group effects appear to be maintained at follow-up. Several moderators of between-group and within-group effects were identified. Risk of bias judgements are reported, and overall heterogeneity was high. Ultra-brief treatments appear to be acceptable and associated with significant symptom improvements. Larger clinical trials with longer follow-up periods are needed.

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