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CompletedNCT074561244FATUpdated Mar 6, 2026

Weight Loss and Adipose Tissue Metabolism During Conservative Treatment of Obesity

An observational study in Obesity & Overweight and Obesity (Disorder), sponsored by University of Helsinki. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-06.

Sponsored by University of Helsinki · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
22
Ages
18 Years and older
Sex
All
01

Study summary

This prospective observational study investigates weight loss and metabolic changes in adults with obesity undergoing standard clinical diet-induced lifestyle treatment and counseling. Participants follow a very-low-calorie diet followed by a conventional weight loss diet in addition to lifestyle counseling and are followed for 12 months. The study examines weight loss as the primary outcome and characterizes changes in body composition, fat distribution, glucose metabolism, inflammation, and adipose tissue biology as secondary outcomes.

Read the detailed description

Obesity is associated with metabolic complications including insulin resistance, fatty liver disease, dyslipidaemia, and systemic inflammation. Weight loss can improve these complications, yet individuals vary widely in weight loss, fat distribution and metabolic response. Subcutaneous adipose tissue dysfunction, including impaired mitochondrial biogenesis and increased inflammation, is thought to play a central role.

This prospective observational study follows adults with obesity undergoing standard-of-care diet and lifestyle treatment at Helsinki University Central Hospital, Helsinki, Finland. The intervention consists of a very-low-calorie diet for approximately 10 weeks, followed by gradual transition to a conventional weight loss diet and multidisciplinary clinical follow-up.

Assessments are performed at baseline, 6 months, and 12 months and include anthropometry, body composition (BIA, DXA), fasting blood samples, and oral glucose tolerance testing. Subcutaneous adipose tissue biopsies are obtained from four anatomical depots (gluteal, abdominal, breast, and upper arm) for molecular, mitochondrial, epigenetic, and histological analyses.

The primary outcome is diet-induced weight loss over 12 months. Secondary outcomes include changes in fat distribution, insulin sensitivity, lipid profile, inflammation, mitochondrial measures in adipose tissue, and depot-specific adipose tissue characteristics.

02

Conditions studied

  • Obesity & Overweight
  • Obesity (Disorder)

Keywords

  • Weight loss
  • obesity
  • adipose tissue
  • inflammation
  • mitochondria
  • metabolism
  • conservative treatment of obesity
  • lifestyle intervention of obesity
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,695 are open to participants now.

This study's enrollment of 22 is below the median of 135 across 1,283 observational studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

University of Helsinki is the lead sponsor of 129 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients seeking treatment for obesity at Helsinki University Central Hospital and affiliated outpatient obesity clinics.

Inclusion criteria

  • Age ≥18 years
  • BMI ≥28 kg/m²
  • Seeking treatment for obesity at Helsinki University Central Hospital or affiliated units

Exclusion criteria

Exclusion Criteria:

  • Pregnancy or lactation
  • Current smoking
  • Anemia (Hb \<130 g/L in men; \<120 g/L in women)
  • Severe comorbid disease or condition judged by investigator to compromise safety
  • Contraindications to MRI (e.g., metal implants, claustrophobia)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
22 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Diet-Induced Weight Loss Cohort

    Adults with obesity undergoing standard clinical diet treatment including a very-low-calorie diet followed by transition to a conventional weight loss diet and lifestyle counseling

    Behavioral: Diet-Induced Weight Loss Program

Interventions

  • BehavioralDiet-Induced Weight Loss Program

    Standard clinical obesity treatment consisting of a very-low-calorie diet for approximately 10 weeks followed by transition to a conventional weight loss diet with multidisciplinary clinical follow-up.

06

What researchers measure

Primary outcomes

  1. Percent Total Body Weight Loss (%TWL)

    Percentage change in body weight from baseline, calculated as 100 × (baseline weight - follow-up weight) / baseline weight

    Time frame: Baseline to 6 months

Secondary outcomes

  1. Change in Body Weight (kg)

    Absolute change in body weight measured in kilograms (kg). Reported as mean change from baseline.

    Time frame: Baseline to 6 and to 12 months

  2. Change in Total Body Fat Mass (kg)

    Change in total body fat mass measured by body impedance analysis (BIA). Reported as mean change from baseline (kg).

    Time frame: Baseline to 6 months and to 12 months

  3. Change in Body Fat percentage (%)

    Change in fat percentage measured by body impedance analysis (BIA). Reported as mean change from baseline (%).

    Time frame: Baseline to 6 and to 12 months

  4. Change in Plasma Glycated Hemoglobin (HbA1c)

    HbA1c plasma glycated hemoglogin measured in SI units mmol/mol, Reported as mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  5. Change in HOMA-IR (Homeostatic Model Assessment of Insulin Resistance)

    HOMA-IR calculated as fasting glucose (mmol/L) × fasting insulin (mU/L) / 22.5. Reported as mean change from baseline.

    Time frame: Baseline to 6 and to 12 months

  6. Change in Plasma Total Cholesterol (mmol/L)

    Change in Plasma Total Cholesterol (mmol/L), Reported as mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  7. Change in Plasma LDL Cholesterol (mmol/L)

    Change in Plasma LDL Cholesterol (mmol/L). Reported as mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  8. Change in Plasma HDL Cholesterol (mmol/L)

    Change in HDL Cholesterol (mmol/L). Reported as mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  9. Change in Plasma Triglycerides (mmol/L)

    Change in Plasma Triglycerides (mmol/L). Reported as mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  10. Change in Plasma C-Reactive Protein Concentration (mg/L)

    Change in Plasma high-sensitivity C-Reactive Protein Concentration (hs-CRP, mg/L). Reported as mean change from baseline.

    Time frame: Baseline, to 6 months and to 12 months

  11. Change in Mitochondrial DNA amount in Subcutaneous Abdominal Adipose Tissue

    Change in Mitochondrial DNA Amount in Subcutaneous Abdominal Adipose Tissue, measured by qPCR as the ratio of mitochondrial to nuclear genes. Reported as a mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  12. Change in Mitochondrial DNA amount in Subcutaneous Breast Adipose Tissue

    Change in Mitochondrial DNA Amount in Subcutaneous Breast Adipose Tissue, measured by qPCR as the ratio of mitochondrial to nuclear genes. Reported as a mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  13. Change in Mitochondrial DNA amount in Subcutaneous Upper Arm Adipose Tissue

    Change in Mitochondrial DNA Amount in Subcutaneous Upper Arm Adipose Tissue, measured by qPCR as the ratio of mitochondrial to nuclear genes. Reported as a mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

  14. Change in Mitochondrial DNA amount in Subcutaneous Lateral Upper Thigh Adipose Tissue

    Change in Mitochondrial DNA Amount in Subcutaneous Lateral Upper Thigh Adipose Tissue, measured by qPCR as the ratio of mitochondrial to nuclear genes. Reported as a mean change from baseline.

    Time frame: Baseline to 6 months and to 12 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Individual participant data are not publicly shared due to data protection regulations; anonymized data may be available upon reasonable request after study completion.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07456124
Lead sponsor
University of Helsinki
Responsible party
Sini Heinonen (Docent in Experimental Internal Medicine, University of Helsinki) — Principal investigator
First posted
Mar 6, 2026
Start date
Aug 19, 2014
Primary completion
Aug 17, 2016
Completion
Aug 17, 2016
Last update
Mar 6, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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