Skip to content

Recovery focused group therapy: Exploring a new treatment for adults with experience of bipolar disorder

Exploring the feasibility and acceptability of a recovery focused group therapy intervention for adults with a bipolar spectrum disorder

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000887471
Enrollment
4
Registered
2016-07-06
Start date
2017-07-15
Completion date
2017-08-02
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Improving support for people with bipolar disorder is an important priority. Worldwide, bipolar disorder causes more pain and suffering than well-known conditions like heart disease and Alzheimer's. Feedback from people with bipolar disorder tells us that recovery is a personal journey about hope, understanding, empowerment and living a meaningful, satisfying and purposeful life alongside their experience of mental health conditions. Even with the right medication, people often have symptoms that continue to affect their everyday lives. Research is needed on an approach that improves individual recovery outcomes and that is useful and easy to access. This study will develop and test an eight session recovery focused group therapy programme for adults with bipolar disorder. An important focus of the project is combining what is currently known about what works with feedback from experts, including consumers. Being recovery focused, the group is an opportunity to learn from one another. Group discussion, activities and at-home tasks will be used to help group members a) increase their awareness of what matters to them; b) strengthen their ability to notice the things they are already doing that bring meaning to their life; c) identify the way(s) they respond when strong thoughts, feelings and/ or sensations show up (to help decide when/ whether these things are useful) and d) take steps towards changing the things that are less helpful in the long run and doing more of the things that bring meaning, purpose and direction. This initial study will involve 24 people with bipolar disorder. All participants will be offered the new group treatment alongside any other treatment they are already using. We will measure key signs (recovery, quality of life, symptoms) several times before and after treatment (baseline, post-treatment and 3 months post-treatment). We will also ask people to give feedback on their experience of participating in the study and the treatment they received. This will help to improve the treatment and inform a larger trial of its use in practice.

Interventions

This recovery focused group therapy will be delivered as an adjunct to existing treatment (pharmacological and/ or psychological). The intervention is informed by Acceptance Based Behavioral Therapy (AABT), motivational interviewing (MI) and consumer feedback. ABBT integrates CBT with principles and strategies from Acceptance and Commitment Therapy (ACT; Hayes, Strosahl & Wilson, 2012), dialectical behavior therapy (DBT; Linehan, 1993) and mindfulness-based cognitive therapy (MBCT; Segal, Willia

This recovery focused group therapy will be delivered as an adjunct to existing treatment (pharmacological and/ or psychological). The intervention is informed by Acceptance Based Behavioral Therapy (AABT), motivational interviewing (MI) and consumer feedback. ABBT integrates CBT with principles and strategies from Acceptance and Commitment Therapy (ACT; Hayes, Strosahl & Wilson, 2012), dialectical behavior therapy (DBT; Linehan, 1993) and mindfulness-based cognitive therapy (MBCT; Segal, Williams & Teasdale, 2002) to address processes implicated in Generalised Anxiety Disorder (GAD; Roemer & Orsillo, 2009). According to this approach, GAD is maintained by an interplay between a) problematic ways of relating to internal experiences (e.g. restricted/ biased attention; critical, negative and fearful stance); b) rigid strategies aimed at experiential avoidance (i.e. efforts to alter the form, frequency and/ or intensity of internal events; Hayes, Wilson, Gifford, Follette & Strosahl, 1996) and c) subsequent ‘behavioral constriction’ (narrowing or avoidance of meaningful/ valued action; Roemer & Orsillo, 2009). This model of ABBT is particularly relevant to the current trial, since as with anxiety, Bipolar Disorder and substance use are also characterized by problematic reactions to internal events (Jones & Day, 2008; Jones, Mansell & Waaller, 2006; Johnson et al. 2008), experiential avoidance and behavioural constriction (Aldao et al., 2010; Spinhoven et al., 2014). The current intervention is designed to promote awareness of (i) how participants respond to experiences related to mood, anxiety and substance use, with a particular emphasis on the role of urges (to avoid, approach and/ or protect) and (ii) the relationship between these responses and valued living. The overarching focus will be on using this awareness to promote increased engagement in meaningful action. Sessions will consist of guided discovery, information provision and exercises (e.g. self-monitoring, mindfulness, awareness of thoughts, feelings and urges). Written material will be used to consolidate key concepts and allow participants to document ‘take home points’ of particular relevance to their own experience. The structure and content of written material will be finalised in collaboration with consumers. Dosage and administration The intervention will comprise eight sessions of face-to-face group therapy, of between 1.5 to 2 hours (plus a 15-30 minute mid-session break) delivered across 8 weeks. All sessions will be led by the same Clinical Psychologist (>10 years experience in research and mental health settings) and co-facilitated by the same Registered Psychologist (>5 years experience, masters level training). Sessions will be held in a community based private psychology clinic located on the Central Coast, NSW. Treatment Integrity Adherence to treatment protocol will be assessed via clinician ratings and separate independent objective rating of audio recorded therapy sessions. At the end of each session, the clinician will complete a rating scale specifically designed for the current study. Audio recordings will be rated using a corresponding fidelity scale specifically designed for the current study (i.e. to assess adherence to and competence in approaches to promote awareness, explore experiential avoidance, facilitate engagement in meaningful action; together with evidence based skills/ strategies for BPSD, anxiety and/ or substance use). This scale will be informed by published recommendations (e.g. Plumb & Roger, 2010; McHugh et al., 2009) and existing fidelity measures applied to ‘third wave’ interventions (e.g. Schimmell-Bristow, Bricker & Comstock, 2012). As we are unsure of how this scale will perform, we may also utilise at least one established instrument for assessing fidelity to CBT (e.g. Cognitive Therapy Scale – revised version). All sessions will be rated by an independent assessor masked to study protocol. To maximise masking, the independent researcher will be located off-site. A 20% sample will be re-rated by a second, independent masked-rater for inter-rater reliability.

Sponsors

Dr Alison Beck
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Aged 18-65 * Meeting DSM-V criteria for BPSD (BP I, BPII, Cyclothymia, Other [Un]Specified) * Able to comprehend English at a level sufficient to complete self-report instruments and clinical interview (i.e. reading age of 12) * Willing to have group therapy sessions audio recorded

Exclusion criteria

* Acute mood episode (as per DSM-V criteria for mania or depression) currently or in the preceding four weeks * Current suicidal ideation with intent * Unable or unwilling to provide informed consent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 25, 2026