Evidence map›Paper›PMID 41359191›Full record

ArticleInternational journal of bipolar disorders2025

Behavioural therapy for inter-episode bipolar symptoms: a multiple baseline case series evaluation.

Kim Wright, Sandra Bucci, Iona Cairns, Barnaby D Dunn, Steven Jones, Heather O'Mahen, Daniel Scott, Rod S Taylor

Abstract read
In one paragraph

Article in International journal of bipolar disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Kim WrightDepartment of Psychology, University of Exeter, Perry Road, Exeter, EX4 4QG, UK. K.A.Wright@exeter.ac.uk.
Sandra BucciDivision of Psychology and Mental Health, School of Health Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Iona CairnsDepartment of Psychology, University of Exeter, Perry Road, Exeter, EX4 4QG, UK.
Barnaby D DunnDepartment of Psychology, University of Exeter, Perry Road, Exeter, EX4 4QG, UK.
Steven JonesDivision of Health Research, Lancaster University, Spectrum Centre for Mental Health Research, Lancaster, LA1 4YT, UK.
Heather O'MahenDepartment of Psychology, University of Exeter, Perry Road, Exeter, EX4 4QG, UK.
Daniel ScottDevon Partnership NHS Trust, Wonford House, Dryden Road, Exeter, EX2 5AF, UK.
Rod S TaylorMRC/CSO Social and Public Health Sciences Unit & Robertson Centre for Biostatistics, School of Health and Well Being, College of Medical, Veterinary and Life Sciences, University of Glasgow, Clarice Pears Building, 90 Byres Road, Glasgow, G12 8TB, UK.

Funding

National Institute for Health and Care Research NIHR302220
6 · The paper itself

Abstract

backgroundBetween major affective episodes some people with bipolar disorder experience persistent low mood or mood instability. Here we report an initial evaluation of the STABILISE programme (ISRCTN19416314; registration date 01.02.23), an adaptation of individual behavioural therapy that includes concepts and techniques addressing emotion regulation designed to support people experiencing these inter-episode symptoms. This study aimed to evaluate the safety, feasibility and acceptability of the intervention and to explore whether the pattern of clinical change had potential for the intervention to be of benefit. Twelve individuals with inter-episode bipolar symptoms received the STABILISE therapy in a randomised, multiple baseline case series. Participants were randomly assigned to wait 3, 4 or 5 weeks before commencing treatment, which comprised up to 22 sessions up to 7 months. Measures of symptoms, mood lability, recovery and quality of life were completed at intake, pre-therapy, and post therapy. Participants completed weekly measures of affective symptoms over the baseline and therapy periods, and for three weeks after.

resultsAll 12 participants completed the therapy programme and reported high levels of satisfaction overall. No adverse events were judged to be therapy related. There was one instance of reliable deterioration on one outcome measure. Across all parameters of clinical change 9 of the 12 participants showed an overall pattern of improvement and none showed a pattern of deterioration overall.

conclusionsThis study provides preliminary support for the feasibility, acceptability, safety, and clinical potential of the STABILISE therapy. Further investigation of these aspects in a larger sample and within a randomised controlled trial design is required.

Indexed as

Behavioural activationBipolar disorderBipolar mood instabilityPsychological therapy

Identifiers

PMID41359191
PMCPMC12811185

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.