Effect of Nutritional Counseling on Anthropometry and Biomarkers in Patients Diagnosed With Schizophrenia/Psychosis or Bipolar Affective Disorder

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVestre Viken Hospital Trust

About this trial

The goal of this clinical trial is to compare the effect of nutritional counseling versus no treatment in patients with schizophenia or bipolar affective disorder.

The main question it aims to answer are:

• Can nutritional counseling have a preventive effect on the development of cardiovascular disease in patients with schizophenia or bipolar affective disorder?

Participants will meet a nutritionist at baseline to asess nutritional status, biochemical and anthropometric measurements. Then, half of the study population will receive nutritional counseling. After six weeks, the same baseline measurements will be repeated to examine any potential differences between the two groups. After the intervention, the control group will be offered the same counseling as the intervention group received during the study.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

> 18 years

Diagnosed with either schizophrenia/psychosis or bipolar affective disorder

Patients treatet in Vestre Viken healthcare company, at either Asker district psychiatric center or Blakstad hospital

Disqualifiers

none

Trial design

Design model

Parallel

Treatments tested in this trial

  • Nutritional counseling

    Behavioral

    The intervention group will recieve 30 x 2 minutes with nutritonal counseling seperatet by a 15 minutes break. The participants will receive individually tailored guidance based on the information recieved at baseline measurments. The couseling will be based on the Norwegian goverments dietary advices and the recommendation from the Directorate of Health for the prevention of cardiovascular diseases.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Non-HDL cholesterol

HDL-cholesterol - total cholesterol, biochemical test

Time frame
6 weeks

Secondary outcomes

1

total cholesterol

biochemical test

Time frame
6 weeks
2

HDL-cholesterol

biochemical test

Time frame
6 weeks
3

Triglycerids

biochemical test

Time frame
6 weeks
4

HbA1c

biochemical test

Time frame
6 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Vestre Viken Hospital Trust

Lead sponsor

University of Oslo

Collaborator