- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06043206
Bariatric Surgery in Patients With Schizophrenia (SCHIZOBAR)
It is known that schizophrenia is associated with obesity in a significant number of patients and it implies a poor prognostic factor, with weight loss being important in this population. However, data about the prognosis of weight loss surgery in subjects with schizophrenia is scant.
Hypothesis: Bariatric surgery in subjects with schizophrenia leads to an improvement in weight and cardiometabolic comorbidities similar to that of subjects without schizophrenia Main goal: To study the evolution after bariatric surgery in patients with obesity and schizophrenia Design: Multicenter retrospective case control study. Disease under study: Schizophrenia and Obesity Methodology: Retrospective observational study Study population and total number of subjects Cases: Patients with schizophrenia and obesity undergoing bariatric surgery. (number: all cases collected within the GOSEEN group).
Controls: Patients without psychiatric pathology matched by age, sex, body mass index and type of surgery and in a 4:1 ratio to cases.
Calendar. Expected duration of the study. 12 months ethical considerations Informed consent will be obtained from patients who are currently being followed up at the reference centers.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
THEORETICAL FRAMEWORK. PROBLEM STATEMENT:
Background Obesity affects approximately 45-55% of patients with schizophrenia (1). Weight gain in these patients may be due to different factors such as the use of antipsychotic drugs with an unfavorable metabolic profile, the coexistence of sleep disorders or negative cognitive symptoms that often translate into a more sedentary lifestyle and alterations in eating behavior, among others (2). The coexistence of obesity and its comorbidities in this group of patients significantly worsens both their physical and mental health (3). In fact, cardiovascular disease is one of the main causes of mortality in patients with schizophrenia (4).
Lifestyle interventions, while they may be effective in people with schizophrenia (5), often fall short of achieving weight goals. At present, obesity surgery represents the most effective treatment in terms of weight loss and resolution of comorbidities, being indicated in cases of patients with a body mass index (BMI) > 35 kg/m2 with comorbidities or BMI > 40 Kg/m2 with/without comorbidities. However, the access of patients with schizophrenia to bariatric surgery techniques is usually limited by different factors such as fear of a possible worsening of the underlying disease, or a lower weight loss in this population, among others. In addition, clinical practice guidelines recommend that all patients with psychiatric pathologies be evaluated in a regulated manner prior to surgery (6), although the content of this evaluation and the criteria for declining or accepting surgery are not clear. Although the course of schizophrenia is variable and its symptoms may be stable without being a clear contraindication for bariatric surgery, in actual practice, a considerable number of professionals contraindicate bariatric surgery in the presence of a psychotic disorder (7).
For these reasons, data on the efficacy of bariatric surgery in patients with schizophrenia are scarce and limited to very small case series with short-term follow-up (2,8,9). Our objective is therefore to carry out a multicenter retrospective study that allows us to study the long-term evolution after bariatric surgery in a large series of patients, focusing not only on weight evolution but also on the long-term evolution of psychiatric pathology.
Justification It is necessary to have information about the prognosis of subjects with severe obesity and schizophrenia who undergo bariatric surgery. This knowledge will make it possible to establish clear guidelines for action in these cases.
Research questions What is the long-term outcome after bariatric surgery in subjects with schizophrenia? Hypothesis Bariatric surgery in subjects with schizophrenia leads to an improvement in weight and cardiometabolic comorbidities similar to that of subjects without schizophrenia
GOALS:
Main goal:
To study the short (first year after bariatric surgery) and long-term (up to 5 years of follow-up after bariatric surgery) evolution in terms of weight loss of patients with obesity and schizophrenia who underwent bariatric surgery in Spain and compare it with the evolution of patients without psychiatric disorder.
Secondary objectives:
- Determine the casuistry of patients, with special interest in the characteristics of the underlying psychiatric pathology (years of evolution, clinical stability criteria, pharmacological treatment...).
- To Analyze the evolution of obesity comorbidities.
- To Analyze the evolution of psychiatric pathology after bariatric surgery: (decompensation, drug treatment...)
- To analyze the frequency of early (<30 days post-surgery) or late (>30 days post-surgery) post-surgical complications.
METHODS:
Study design Retrospective case-control study.
Expected sample size All cases detected in Spanish territory The minimum number of cases expected will be 10 patients based on the low casuistry of the problem. The number of patients in the control group will be x4 that in the study group.
Methodology. Information sources The study population will be identified in each center in the usual specialty consultations or by searching the databases of each center. Review of medical records in search of the specified variables (retrospective observational study).
Data Management and Analysis The coordinating researcher (Dra Inka Miñambres Donaire) will be responsible for the creation of the database and its exploitation. The database will be created in Excell format and the SPSS program will be used for statistical analysis. The statistics will be mainly descriptive. For cases in which it is decided to compare groups, normality tests will be used to establish the behavior of the variables and parametric/non-parametric tests will be used as appropriate.
Data collection The researcher will guarantee the accuracy and integrity of the data, as well as all the reports that are required. The data included in the Data Collection Notebook (CRD), which are derived from source documents, will be consistent with those documents or otherwise the discrepancies will be justified.
The researcher will keep the study documents until at least 5 years after completion.
At the request of the monitor, auditor, ethics committee or health authority, the researcher will have available all the files related to the study, allowing direct access to the data or source documents for monitoring, auditing, review by the ethics committee, as well as the inspection of the trial by the competent authorities.
Limitations of the design, the source of information and the methods of analysis
The main limitation of the study is its retrospective nature. However, the study design is adequate given the low frequency of the pathology.
Data confidentiality Regarding the confidentiality of the study data, the provisions of Organic Law 3/2018, of December 5, on the Protection of Personal Data and Guarantee of Digital Rights and the General Regulation (EU) on Data Protection will be followed. 2016/679.
Interference with physician's prescribing habits As it is a retrospective study, there will be no interference with the prescribing habits of the doctor.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Barcelona, Spain, 08025
- Hospital of Santa Creu i Sant Pau
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Cases:
Inclusion) Both criteria must be met:
- Patients with severe obesity undergoing bariatric surgery and with follow-up in Spanish territory.
- Patient with schizophrenia or schizoaffective disorder.
Exclusion) Subjects who do not meet any of the two inclusion criteria
Controls: in a 4:1 ratio with cases
Inclusion) Both criteria must be met:
- Patients with severe obesity undergoing bariatric surgery and with follow-up in Spanish territory.
- Absence of psychiatric pathology
- Paired with the cases by age, sex, BMI before surgery and type of surgery.
Exclusion) Subjects who do not meet any of the two inclusion criteria
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Cases Obesity and schizophrenia
Patients with schizophrenia and obesity undergoing bariatric surgery
|
Bariatric Surgery
|
Controls
Patients without psychiatric pathology matched by age, sex, BMI and type of surgery and in a 4:1 ratio to cases.
|
Bariatric Surgery
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Weight loss
Time Frame: 12 months and 5 years after the surgery
|
short (first year after bariatric surgery) and long-term (up to 5 years of follow-up after bariatric surgery) evolution in terms of weight loss of patients with obesity and schizophrenia who underwent bariatric surgery
|
12 months and 5 years after the surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clincial Caracteristics description
Time Frame: inclusion, day 1
|
casuistry of patients, with special interest in the characteristics of the underlying psychiatric pathology (years of evolution, clinical stability criteria, pharmacological treatment...)
|
inclusion, day 1
|
Comorbidity progression
Time Frame: 12 months and 5 years after the surgery
|
Analyze the evolution of obesity comorbidities: presence of type 2 diabetes, hypertension, OSAS and dyslipidemia.
Remission of co morbidities was defined as cessation of medication for hypertension or hyperlipidemia with normal blood pressure and lipid levels, cessation for continuous positive pressure ventilation for sleep apnea, and normalization of HbA1C (<6.5) with no medications for diabetes.
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12 months and 5 years after the surgery
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Psychiatric pathology progression
Time Frame: 30 days post surgery and 5 years after the surgery
|
Analyze the evolution of psychiatric treatment: Psychiatric medication burden will be calculated by generating a continuous variable using a previous validated formula (Central Nervous System Medication Burden and Serious Falls in Older Nursing Home Residents Joseph T. Hanlon, J Am Geriatr Soc.
2017 June ; 65(6): 1183-1189.
doi:10.1111/jgs.14759).
|
30 days post surgery and 5 years after the surgery
|
post-surgical complications
Time Frame: up to 30 days post-surgery) or late post-surgical complications (through study completion, up to five years post-surgery)
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To analyze the frequency of early or late post-surgical complications
|
up to 30 days post-surgery) or late post-surgical complications (through study completion, up to five years post-surgery)
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Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IIBSP-BAR-2022-30
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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