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PROgram To Enhance Cardiovascular Risk Trough an Intervention of Nutrition in Bipolar Disorder

The Effect of a Nutritional Intervention Focused on Dietary Pattern in the Cardiovascular Risks of Individuals With Bipolar Disorder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06488573
Acronym
PROTECTION-BD
Enrollment
88
Registered
2024-07-05
Start date
2026-04-01
Completion date
2027-12-01
Last updated
2026-03-02

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

Conditions

Bipolar Depression, Bipolar Disorder (BD)

Keywords

nutrition intervention, nutritional psychiatry, bipolar disorder, dietary intervention, brazilian dietary guideline

Brief summary

Individuals with Bipolar Disorder (BD) have twice the risk of being affected by metabolic comorbidities and a 1.8-fold increased risk of mortality from cardiovascular diseases when compared to the general population. These factors are fundamental in the 14-year reduction in the life expectancy of people with TB reported in recent meta-analyses. This occurs mainly due to the increased inflammation associated with the disease, the adverse effects of pharmacological treatments and unhealthy lifestyle habits that are more common in people diagnosed with BD. Nutrition has been studied as an adjunctive treatment in other psychiatric disorders, but there is a lack of studies about the role of nutrition in TB. Considering that diet can impact metabolic health, this randomized controlled study aims to evaluate the effect of a nutritional intervention on cardiovascular risk in patients with TB. The intervention is based on the dietary pattern recommended in the Dietary Guidelines for the Brazilian Population and will be applied by a registered dietitian. According to the literature, the sample size will be 72 individuals with TB (36 in the control group with usual treatment + 36 in the intervention group added to the usual treatment). The intervention will be carried out in 7 individual sessions and 8 group sessions with specific themes. The primary aim of this protocol will be an intervention to contribute to cardiovascular health - verified by serum markers, anthropometric measurements and the Framingham Cardiovascular Risk Score (algorithm used to estimate an individual's 10-year cardiovascular risk). The secondary stages will be the adherence of the intervention and the impact on the quality of life of the participants. The possible positive results of this nutritional intervention can open new clinical perspectives. Meaning that might show that better food choices can protect the cardiovascular health of individuals with TB, leading to a reduction in morbidity and mortality associated with the disease.

Interventions

BEHAVIORALNutritional intervention

7 individual sessions (online) + 6 small group sessions (1-in person + 5 online)

Sponsors

University of Sao Paulo
Lead SponsorOTHER
Deakin University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Control group vs intervention group

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of Bipolar disorder types I and II diagnosis * Adults of both genders, from 18 to 60 years old * In typical pharmacotherapy for BD, for at least one month * Agreement to participate in the study with signature of the consent form

Exclusion criteria

* Patients with "very good or excellent" diet quality assessed by the diet quality scale (ESQUADA): \>275 out of a score of 375 * Patients in a state of hypomania or mania: score \>8 (Young Mania Rating Scale - YMRS) * Patients with severe depression \>21 Montgomery-Åsberg Depression Rating Scale * Patients at low cardiovascular risk (\<7 points for men or \<9 points for women on the Framingham Global Risk Score) * Low weight or eutrophic body mass index: \<25kg/m² as in similar studies * Pregnant or breastfeeding women * Patients diagnosed with anorexia and bulimia nervosa * Patientes diagnosed with Irritable Bowl Syndrome or other diagnosed conditions that affect the gastrointestinal function

Design outcomes

Primary

MeasureTime frameDescription
waist circumferenceBaseline, week 12, week 24 and follow up at week 52waist circumference
C reactive proteinBaseline, week 12, week 24 and follow up at week 52C reactive protein
Total cholesterol and fractionsBaseline, week 12, week 24 and follow up at week 52Total cholesterol and fractions
GlycemiaBaseline, week 12, week 24 and follow up at week 52Glycemia
Glycated hemoglobin A1CBaseline, week 12, week 24 and follow up at week 52Glycated hemoglobin A1C
TriglyceridesBaseline, week 12, week 24 and follow up at week 52Triglycerides
HOMA IRBaseline, week 12, week 24 and follow up at week 52HOME IR
Apoliporpotein BBaseline, week 12, week 24 and follow up at week 52Apoliporpotein B
Cardiovascular riskBaseline, week 12, week 24 and follow up at week 52Framingham Global Risk Score (-3 to 21; higher scores mean worse outcome)
Body weightBaseline, week 12, week 24 and follow up at week 52Body weight
Body fat percentageBaseline, week 12, week 24 and follow up at week 52Body fat percentage

Secondary

MeasureTime frameDescription
Dietary assessment - dietary intakeBaseline, week 12, week 24 and follow up at week 523-day food record from last week (calories and macronutrients)
Dietary assessment - dietary qualityBaseline, week 12, week 24 and follow up at week 52ESQUADA (0-375; higher scores mean better outcome)
Dietary assessment - dietary adehrenceBaseline, week 12, week 24 and follow up at week 52NUTRINET (0-72; higher scores mean worse outcome)
Quality of life WHOQOLBaseline, week 12, week 24 and follow up at week 52WHOQOL Bref Portuguese (0-100; higher scores mean better outcome)

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026