Waist Circumference Measurements in Schizophrenic Patients
NCT ID: NCT01243034
Last Updated: 2019-02-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
80 participants
OBSERVATIONAL
2010-08-01
2011-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Objectives: 1. To compare the magnitude of WC measured at 3 sites ( immediately above the iliac crest, midpoint between the lowest rib and the iliac crest , umbilical level) in males and females.
2\. To examine the correlation of WC with Triglyceride, cholesterol, HDL, LDL and glucose.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Prevalence of Obesity For Schizophrenia Inpatients in Taiwan
NCT01170689
Prevalence of and Factors Associated With Metabolic Syndrome in Schizophrenia
NCT01587521
The Effectiveness of Lower Extremity Strength Training
NCT07183969
Feasibility and Preliminary Effect of Baduanjin Program for People Diagnosed With Schizophrenia
NCT04027634
Coronary Artery Disease in Patients Suffering From Schizophrenia
NCT02885792
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Body weight change less than 1 kg in previous one month before index date.
Exclusion Criteria
* Patients received any anti-hypertensives or oral hypoglycemic agents.
* Pregnant or breast-feeding women.
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Changhua Christian Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Cheng-Chen Chang
attending psychiatrist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Changhua Christian Hospital
Changhua, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
100717
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.