A Compassionate-focused Intervention for Older People with Bipolar Disorder (NCT06882590) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
A Compassionate-focused Intervention for Older People with Bipolar Disorder
United Kingdom6 participantsStarted 2025-07-01
Plain-language summary
The aim of this study is to determine whether it is feasible to deliver a 9-session compassionate-focused therapy for older people with bipolar disorder. Participants will be asked to complete baseline measures and at post-intervention follow-up (12 weeks and 24 weeks) to understand any potential clinical benefits of the therapy.
Who can participate
Age range
60 Years – 90 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adults aged 60 years and above.
* Have a nominated healthcare professional (i.e. GP/Care Coordinator)
* Meet the criteria for a diagnosis of bipolar disorder I or II according to the MINI.
* Score of \>57 on Ruminative Response Scale (RRS)
* Be able to provide written informed consent.
* Be able to speak sufficient English to engage in the assessments and intervention.
Exclusion Criteria:
* Currently in an episode of mania or hypomania according to the MINI.
* Experiencing 'severe depression' according to the Hamilton Depression Rating Scale, which equates to a score of over 24.
* MoCA score of \<22 to exclude for moderate and severe cognitive impairment.
* Currently receiving psychological therapy.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Number of therapy sessions attended
Timeframe: The timeframe for number of therapy sessions attended will span the length of intervention; from the first assessment session to final therapy session. The estimated period of time over which the event is assessed is up to 9 weeks.
2
Number of participants who drop-out and at which stage of the intervention
Timeframe: The time frame covers first therapy session to final therapy session. The estimated period of time over which the event is assessed is up to 9 weeks.