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Body Weight Reduction and Metabolic/Biochemical Parameters in Overweight or Obesity

The Effect of Body Weight Reduction on Selected Metabolic and Biochemical Parameters in Individuals With Overweight or Obesity

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07645105
Enrollment
53
Registered
2026-06-12
Start date
2016-05-10
Completion date
2022-09-30
Last updated
2026-06-12

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

Conditions

Abdominal Obesity-Metabolic Syndrome, Overweight , Obesity

Keywords

body weight reduction, overweight, obesity, abdominal obesity, metabolic syndrome, body composition, glucose metabolism, lipid metabolism, oxidative stress, inflammatory markers, adipokines, cytokines

Brief summary

This was a single-center prospective observational cohort study conducted in Poland in the context of routine metabolic outpatient care. The study assessed selected metabolic, biochemical, oxidative-stress, inflammatory, and body-composition parameters in individuals with overweight or obesity undergoing standard lifestyle-based body weight reduction management. Participants with BMI \> 25 kg/m² were followed before and after body weight reduction, while individuals with normal body weight served as a comparison group. The weight reduction management included individualized dietary recommendations, physical-activity guidance, health education, regular follow-up visits, fasting blood sampling, and body-composition assessment. The aim of the study was to evaluate whether body weight reduction is associated with changes in metabolic and biochemical parameters, with particular attention to glucose and lipid metabolism, oxidative stress, inflammatory markers, adipokines, cytokines, and body-composition changes.

Detailed description

This was a single-center prospective observational cohort study conducted at the Medical University of Silesia in Katowice, Poland, and in a metabolic outpatient clinic in Miasteczko Śląskie, Poland. The study was designed to evaluate the effect of body weight reduction on selected metabolic, biochemical, oxidative-stress, inflammatory, and body-composition parameters in individuals with overweight or obesity. The study was conducted in the context of routine metabolic outpatient care. Participants with overweight or obesity received standard lifestyle-based body weight reduction management, including individualized dietary recommendations, physical-activity guidance, health education, and regular follow-up visits. The investigators did not assign participants to an investigational medicinal product, medical device, dietary supplement, surgical procedure, pharmacological intervention, or experimental therapy. The study prospectively observed participants receiving routine lifestyle-based weight reduction management and assessed changes in clinical and laboratory parameters before and after body weight reduction. The approved study protocol planned the inclusion of individuals with overweight or obesity and a normal-weight comparison group. Participants with BMI \> 25 kg/m² were evaluated in relation to body weight reduction, while individuals with normal body weight served as a comparison group for selected baseline analyses. Patients with overweight or obesity were assessed by medical examination, dietary and clinical questionnaires, anthropometric measurements, body-composition analysis, and fasting blood sampling. Body-composition analysis included assessment of body weight, fat mass, fat-free mass, skeletal muscle mass, total body water, visceral fat, and related parameters. Blood samples were collected for biochemical analyses, including markers of glucose metabolism, lipid metabolism, oxidative stress, antioxidant status, inflammatory markers, adipokines, cytokines, chemokines, growth factors, and selected cardiovascular-risk parameters. Participants with overweight or obesity were followed during standard body weight reduction management until clinically relevant weight reduction or achievement of optimal body weight. According to the original study documentation, assessments were planned before the start of weight reduction, after approximately 10% body weight reduction, and after approximately 20% body weight reduction or achievement of target body weight. Follow-up visits included body weight measurements, waist and hip circumference measurements, dietary counselling, education regarding caloric intake, and motivation to continue lifestyle modification. The primary objective of the study was to assess whether body weight reduction in individuals with overweight or obesity is associated with changes in selected metabolic and biochemical parameters. Secondary objectives included evaluation of oxidative-stress and antioxidant-status parameters, glucose and lipid metabolism, inflammatory markers, adipokines, cytokines, and body-composition changes. The study also aimed to assess relationships between biochemical parameters and body-composition indices before and after body weight reduction. The study was approved by the Bioethics Committee of the Medical University of Silesia in Katowice, Poland. All participants received information about the study and provided written informed consent before participation. This ClinicalTrials.gov record is submitted retrospectively to meet journal publication requirements and to provide transparent public information about the completed study.

Interventions

BEHAVIORALRoutine Lifestyle-Based Weight Reduction Management

Standard lifestyle-based body weight reduction management received as part of routine metabolic outpatient care. It included individualized dietary recommendations, physical-activity guidance, health education, and regular follow-up visits. Participants were not assigned to this management as part of the study; the study prospectively observed patients receiving routine care and assessed metabolic, biochemical, inflammatory, oxidative-stress, adipokine, cytokine, and body-composition parameters before and after body weight reduction.

Sponsors

Medical University of Silesia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18-85 years * BMI \> 25 kg/m² * Overweight or obesity diagnosed on the basis of medical examination and body-composition assessment * Participation in routine lifestyle-based body weight reduction management in a metabolic outpatient clinic * Written informed consent to participate in the study

Exclusion criteria

* Lack of informed consent * Severe hepatic insufficiency * Severe renal insufficiency * Severe respiratory insufficiency * Severe circulatory insufficiency * Disturbances of consciousness * Treatment-resistant depression * Chronic alcohol abuse * Pregnancy * History of serious nervous system injury * Implanted cardiac pacemaker * Pharmacological treatment affecting glucose and/or lipid metabolism * Incomplete follow-up or incomplete laboratory data

Design outcomes

Primary

MeasureTime frameDescription
Change in Body WeightBaseline and after body weight reduction, up to approximately 6 monthsChange in body weight from baseline to follow-up after routine lifestyle-based body weight reduction management.

Secondary

MeasureTime frameDescription
Change in Body Fat MassBaseline and after body weight reduction, up to approximately 6 monthsChange in body fat mass assessed by bioelectrical impedance analysis and expressed in kilograms.
Change in Glucose concentration in mg/dl.Baseline and after body weight reduction, up to approximately 6 monthsChanges in fasting glucose.
Change in total-cholesterol concentration in mg/dl.Baseline and after body weight reduction, up to approximately 6 monthsChanges in total cholesterol concentration.
Change in malondialdehyde concentration in μmol/l.Baseline and after body weight reduction, up to approximately 6 monthsChange in blood malondialdehyde concentration, assessed as a marker of lipid peroxidation and oxidative stress, from baseline to follow-up after body weight reduction.
Change in serum IL-6 concentration in pg/ml.Baseline and after body weight reduction, up to approximately 6 monthsChange in serum interleukin-6 (IL-6) concentration from baseline to follow-up after body weight reduction. IL-6 was measured in serum samples as a marker of systemic low-grade inflammation and expressed in pg/ml.

Countries

Poland

Contacts

PRINCIPAL_INVESTIGATORSławomir Kasperczyk, Prof

Medical University of Silesia in Katowice

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 20, 2026