Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06624462

Effectiveness of a Pragmatic, Metabolic Care Clinic for Patients With Severe Mental Illness - The Meta Care Clinic

This study will examine the effectiveness of a Pragmatic, Metabolic Care Clinic for Patients With Severe Mental Illness

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre for Neuropsychiatric Schizophrenia Research, CNSR, Mental Health Centre Glostrup

Glostrup Municipality, Capital Region, 2600, Denmark

Location status: Recruiting

Location contact

Bjorn H Ebdrup, MD, Consultant,PhD, Professor,

CONTACT

[email protected]

+4538640840

Grimur H Mohr, MD

CONTACT

[email protected]

+45 38 64 08 40

About this study

Severe mental illness (SMI), including schizophrenia spectrum disorders and bipolar disorder, is associated with high mortality rates and cardiovascular disease. Obesity and dysmetabolism caused by antipsychotic medication comprise modifiable risk factors, which remain undertreated.

The investigators will address the gaps in cardiometabolic care of SMI patients by examining the effectiveness of a pragmatic metabolic care clinic for patients with SMI. Moreover, the investigators will include qualitative investigation of patients' perspectives in relation to acceptability, satisfaction with care, and motivation for health behaviour change.

A total of 84 patients between 18-45 years with diagnoses of schizophrenia spectrum disorders or bipolar disorder will be recruited from inpatient and outpatient clinics in the Mental Health Services of the Capital Region of Denmark. Eligible patients are antipsychotics-treated and present with a 5% weight increase / 5 cm waistline increase since initiation of antipsychotic therapy or body mass index (BMI) ≥30 kg/m2 or BMI ≥27 kg/m2 and concomitant prediabetes, diabetes, hypertension, sleep apnoea and/or dyslipidaemia.

Patients will be enrolled in an open-label randomized controlled parallel-group trial with an allocation-ratio of 1:1 to a pragmatic, specialized metabolic clinic with measurement-based care and evidence-based best-practice treatment or standard care. The primary outcome is the proportion of patients in the intervention group achieving a weight loss ≥5% of initial body weight vs the standard care group at 12 months. Secondary and exploratory outcomes include changes in other cardiovascular risk factors, quality of life, personal recovery and cognitive measures. Finally, qualitative interviews will explore patient experience and contextual factors.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with schizophrenia spectrum disorders (International classification of diseases; ICD-10: DF2x) or bipolar disorder (ICD-10: DF30.x or DF31.x)
  • Medical treatment with antipsychotics
  • Age 18-45 years
  • Legally competent
  • Able to give informed consent

and either:

  • Body mass index (BMI) ≥30 kg/m2.

Or

  • BMI ≥27 kg/m2 and at least one of the following:
  • Hypertension defined as treatment with ≥1 antihypertensive drug or out-of-office / 24-hour, non-invasive ambulatory blood pressure ≥140/90 mmHg within the previous 6 months
  • Dyslipidaemia defined as treatment with ≥1 lipid-lowering drug or elevated low-density lipoprotein (LDL) cholesterol (≥3.0 mmol/l), elevated triglycerides (≥1.7 mmol/l) or low high-density lipoprotein cholesterol (≥1.2 mmol/l in women and ≥1.0 mmol/l in men) within the previous 6 months
  • Sleep apnoea (ICD-10 DG473).
  • Prediabetes or diabetes defined as HbA1c ≥42 mmol/mol or impaired fasting glucose as defined by the International Diabetes Federation within the previous 6 months.

Or

  • a history of rapid weight gain during antipsychotic therapy defined as increases of either ≥5% body weight or ≥5 cm waist circumference since initiation of antipsychotic therapy.

Exclusion criteria

  • Clinical or laboratory evidence of comorbid medical disease not compatible with participation as judged by the research team.
  • Unstable psychiatric disorder as judged by the research team.
  • Severe current drug or alcohol misuse as judged by the research team.
  • Acute suicidal risk.

Treatment and study plan

Treatment in the Meta Care Clinic

Other
  • Consultations by medical doctors with specific metabolic training from the metabolic clinic located at Centre for Addiction and Mental Health in Toronto, Canada, and an exercise physiologist.
  • Evaluation of their psychopharmacotherapy with consultation and detailed recommendations to the patients' treating psychiatrist and/or general practitioner regarding dosage reductions or switching of psychotropics if this is clinically feasible to reduce the metabolic burden.
  • Lifestyle interventions
  • Pharmacotherapy with evidence to support use to mitigate antipsychotic-induced weight gain
  • Treatment of other cardiovascular risk factors such as dyslipidaemia, hypertension, smoking and diabetes in close collaboration with recognized specialists in endocrinology.
  • Assessment of plans at conferences with participation of the sponsor, the primary investigator as well as recognized specialists in endocrinology and psychiatry.
  • Qualitative interviews will be conducted post-intervention.

Standard care with general practitioner and/or outpatient clinics

Other

Following measurements after 12 months, patients will receive individualized lifestyle recommendations from an exercise physiologist and a MD will offer to send recommendations regarding the following potential post-trial interventions to the patients' general practitioner and/or outpatient clinic prepared in close collaboration with recognized specialists in psychiatry and endocrinology:

  • Suggestions regarding relevant psychotropic medication adjustments or switches if this is found relevant and clinically feasible to reduce the metabolic burden.
  • Suggestions regarding potential add-on of weight reducing pharmacotherapy.
  • Suggestions regarding pharmacological treatment of other cardiovascular risk factors such as dyslipidaemia, hypertension, smoking and type 2 diabetes.

Primary outcomes

  1. Proportion of patients achieving a weight loss of ≥5% of initial body weight.

    Time frame: 12 months

    Proportion of patients in the intervention group achieving a weight loss of ≥5% of initial body weight vs the standard care group at 12 months.

Secondary outcomes

  1. The metabolic composite score

    Time frame: 12 months

    The metabolic composite score consisting of minimally 0 points and maximally five points (one point per composite; elevated waist circumference, elevated triglycerides, blood pressure, fasting plasma glucose, and reduced high-density lipoprotein), according to the definition and cut-off values of metabolic syndrome by the International Diabetes Federation. A higher score means worse outcomes. Effect measurements: differences in percentage achieving reduction of ≥1 points between groups at 12 months.

  2. Cardiovascular risk factors

    Time frame: 12 months

    Cardiovascular risk factors as defined below.

  3. Proportion of patients achieving a weight loss of ≥10% of initial body weight.

    Time frame: 12 months

    Proportion of patients in the intervention group achieving a weight loss of ≥10% of initial body weight vs the standard care group at 12 months.

  4. Proportion of patients achieving a ≥50% reduction of low-density lipoprotein cholesterol

    Time frame: 12 months

    Proportion of patients in the intervention group achieving a ≥50% reduction of initial low-density lipoprotein cholesterol vs the standard care group at 12 months.

  5. Body weight

    Time frame: 12 months

    Absolute and relative changes in body weight. Effect measurements: differences in mean changes between groups at 12 months.

  6. Waist circumference

    Time frame: 12 months

    Absolute and relative changes in waist circumference. Effect measurements: differences in mean changes between groups at 12 months.

  7. Body mass index

    Time frame: 12 months

    Changes in body mass index (BMI) where weight and height will be combined to report BMI in kg/m^2. Effect measurements: differences in mean changes between groups at 12 months.

  8. Glucose

    Time frame: 12 months

    Fasting plasma glucose. Effect measurements: differences in mean changes between groups at 12 months.

  9. Insulin

    Time frame: 12 months

    Fasting Plasma insulin. Effect measurements: differences in mean changes between groups at 12 months.

  10. The homeostatic Model Assessment for Insulin Resistance

    Time frame: 12 months

    The homeostatic Model Assessment for Insulin Resistance (HOMA-IR) measured using fasting plasma glucose and fasting plasma insulin.

    Effect measurements: differences in mean changes between groups at 12 months.

  11. Total cholesterol

    Time frame: 12 months

    Fasting plasma total cholesterol. Effect measurements: differences in mean changes between groups at 12 months.

  12. Low-density lipoprotein cholesterol

    Time frame: 12 months

    Fasting plasma Low-density lipoprotein (LDL) cholesterol. Effect measurements: differences in mean changes between groups at 12 months.

  13. High-density lipoprotein cholesterol

    Time frame: 12 months

    Fasting plasma high-density lipoprotein (HDL) cholesterol. Effect measurements: differences in mean changes between groups at 12 months.

  14. Very Low-density lipoprotein cholesterol

    Time frame: 12 months

    Fasting plasma Very Low-density lipoprotein (VLDL) cholesterol. Effect measurements: differences in mean changes between groups at 12 months.

  15. Triglycerides

    Time frame: 12 months

    Fasting plasma triglycerides. Effect measurements: differences in mean changes between groups at 12 months.

  16. Heart rate

    Time frame: 12 months

    Resting heart rate. Effect measurements: differences in mean changes between groups at 12 months.

  17. Blood pressure

    Time frame: 12 months

    Clinic blood pressure. Effect measurements: differences in mean changes between groups at 12 months.

  18. Hemoglobin A1c

    Time frame: 12 months

    Hemoglobin A1c (HbA1c). Effect measurements: differences in mean changes between groups at 12 months.

Other outcomes

  1. Cardiorespiratory fitness

    Time frame: 12 months

    Cardiorespiratory fitness assessed by the submaximal Ekblom-Bak test on a mechanically braked cycle ergometer. Effect measurements: differences in mean changes between groups at 12 months.

  2. Body composition: Total body fat percentage

    Time frame: 12 months

    Total body fat percentage measured with a bioelectrical impedance analysis. Effect measurements: differences in mean changes between groups at 12 months.

  3. Body composition: Visceral adipose tissue

    Time frame: 12 months

    Visceral adipose tissue measured with a bioelectrical impedance analysis. Effect measurements: differences in mean changes between groups at 12 months.

  4. Body composition: Skeletal muscle mass.

    Time frame: 12 months

    Skeletal muscle mass measured with a bioelectrical impedance analysis. Effect measurements: differences in mean changes between groups at 12 months.

  5. Personal recovery - The Brief INSPIRE Measure of Staff Support for Personal Recovery.

    Time frame: 12 months

    The Brief INSPIRE Measure of Staff Support for Personal Recovery. Effect measurements: differences in mean changes between groups at 12 months.

  6. Personal recovery - The Questionnaire about the Process of Recovery.

    Time frame: 12 months

    The Questionnaire about the Process of Recovery (QPR). Effect measurements: differences in mean changes between groups at 12 months.

  7. Quality of life - the World Health Organization-5 Well-being index.

    Time frame: 12 months

    The World Health Organization (WHO)-5 Well-being index. Effect measurements: differences in mean changes between groups at 12 months.

  8. Cognition - The Symbol Digit Modalities Test (SDMT).

    Time frame: 12 months

    The Symbol Digit Modalities Test (SDMT). Effect measurements: differences in mean changes between groups at 12 months.

  9. Cognition - The Brief Cognitive Assessment Tool in Schizophrenia

    Time frame: 12 months

    The Brief Cognitive Assessment Tool in Schizophrenia (B-CATS) comprised of the following:

    • The Trail Making Test.
    • The Letter-Number Span Record Form.
    • The Category Fluency Test.

    Effect measurements: differences in mean changes between groups at 12 months.

  10. Smoking Cessation

    Time frame: 12 months

    Smoking cessation amongst persons who are smoking at baseline measured as self-reported cessation for the past 7 days after 12 months. Effect measurements: differences in mean changes between groups at 12 months.

  11. Physical activity

    Time frame: 12 months

    Physical activity of weekly self-perceived volumes of different intensities and average daily sedentary hours measured with the International Physical Activity Questionnaire. Effect measurements: differences in mean changes between groups at 12 months

  12. Appetite

    Time frame: 12 months

    Appetite measured with a digital visual analogue scale (VAS) before the first meal at date of baseline measurements and date of measurements after 12 months as minimum 1 and maximally 10 with higher outcomes depicting more appetite. Effect measurements: differences in mean changes between groups at 12 months.

  13. Qualitative evaluation

    Time frame: Time from study start to dropout or 12 months

    Semi-structured interviews will be conducted following the intervention with patients, who dropped out or completed the intervention, respectively. Patients who complete the intervention will be sampled purposefully to ensure maximum variation in terms of gender, age, and diagnosis, whereas the investigators will interview every patient dropping out (i.e., convenience sampling). Interviews will focus on satisfaction with the delivered care, and sustained motivation for health behaviour change. Data will be analysed by means of inductive-deductive thematic analysis informed by the COM-B model identifying capability, opportunity, and motivation as key factors which need to change in order for a behaviour change intervention to be effective. Adequate sample size for the qualitative evaluation will be guided by information power (also denoted saturation).

Study contacts

Contact information is provided by the study sponsor or research team.

Bjorn H. Ebdrup, MD, Consultant,PhD, Professor,

CONTACT

[email protected]

+4538640840

Sponsors and collaborators

Lead sponsor

Bjorn H. Ebdrup

Other

Collaborators

  • Glostrup University Hospital, Copenhagen
  • Herlev and Gentofte Hospital
  • University of Toronto

Registry information

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Oct 3, 2024
Registry last updated
Jan 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.