A study protocol for the feasibility and acceptability of a personalized early intervention combining light therapy, lifestyle psychoeducation, and imagery-focused cognitive therapy in individuals at risk for bipolar disorder

🎖️ Top 10% JournalJan 22, 2026International journal of bipolar disorders

Testing a personalized early treatment with light therapy, lifestyle education, and mental imagery therapy for people at risk of bipolar disorder

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Abstract

Fifty participants aged 16-35 years identified as at risk for bipolar disorder will be included in a novel early intervention program.

The intervention combines bright light therapy, lifestyle psychoeducation, and imagery-focused cognitive therapy.
Feasibility and acceptability will be assessed through drop-out rates, adherence, and participant feedback.
Secondary outcomes include changes in symptoms related to depression, hyperactivity, anxiety, and mental imagery.
The study aims to inform preventive strategies for individuals in an at-risk mental state for bipolar disorder.
Data collected may guide future randomized controlled trials and the integration of early interventions into routine mental health services.

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BACKGROUND: Bipolar disorder (BD) is a severe mental illness associated with marked functional impairment and reduced life expectancy. Early indicators such as mood instability, circadian rhythm disturbance, and anxiety symptoms often precede the first manic or depressive episode, providing a potential window for preventive intervention. Currently, no structured early intervention program exists for individuals at risk for BD who do not yet meet diagnostic criteria. This study aims to evaluate the feasibility and acceptability of a novel, personalized early intervention program combining light therapy, lifestyle psychoeducation, and imagery-focused cognitive therapy (ImCT) for individuals at risk for BD.

METHODS: The study employs a single-case experimental A-B-A design with staggered baseline and multiple daily assessments. Fifty participants aged 16-35 years identified as being at risk for BD by a specialized early detection team will be included. The intervention consists of three core components: (1) a chronotherapeutic intervention (bright light therapy or blue-light blocking glasses) tailored to individual symptom profiles; (2) one session of lifestyle-focused psychoeducation targeting sleep, nutrition, and physical activity; and (3) six sessions of ImCT to address mood instability and maladaptive mental imagery. Feasibility and acceptability will be assessed through drop-out rates, adherence, and participant feedback. Secondary outcomes include changes in depressive, hyperactive, anxiety, and imagery-related symptoms, as well as sleep quality and activity levels, measured through validated questionnaires and actigraphy.

DISCUSSION: By combining chronotherapeutic, psychological, and lifestyle components, this intervention targets multiple mechanisms implicated in BD risk. Findings will inform the development of preventive strategies for individuals in an at-risk mental state for BD. The study will also provide data on the feasibility of integrating early interventions within routine mental health services and guide the design of future randomized controlled trials.

TRIAL REGISTRATION: Medical Ethical Committee Brabant (METC Brabant; identifier P2314); ClinicalTrials.gov Identifier: NCT06282250. Registered 20 February 2024.

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