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Effect of Protein Source During Ketogenic Weight Loss Intervention

Not Applicable
Active, not recruiting
Conditions
Obesity; Endocrine
Obesity
Interventions
Dietary Supplement: Protein supplement - Plant protein
Dietary Supplement: Protein supplement - Animal protein
Registration Number
NCT06461806
Lead Sponsor
Concordia University, Montreal
Brief Summary

This randomized, controlled, single-blinded study will investigate how the protein source in a high-protein ketogenic diet affects metabolic weight loss outcomes after a 12-week dietary intervention

Detailed Description

This randomized, controlled, single-blinded study will compare how a ketogenic weight loss diet, supplemented with either animal- or plant-based protein affects: (i) metabolic markers (adipokine and cytokine) in adipose tissue and blood, (ii) adipose tissue immune cell profiles, and (iii) adipocyte characteristics and their interaction with other cells (e.g. immune cells and muscle cells). To better determine how tissue characteristics affect the whole body level, the relationships between adipose tissue characteristics and blood lipid and inflammatory markers will also be examined. Participants undergo anthropometric measurements, questionnaires, body composition assessment, energy assessment, blood draws, and adipose tissue biopsies from the abdominal and femoral adipose tissue depots

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Adults between 18-60 years old
  • BMI: >29.99kg/m2
Exclusion Criteria
  • Any chronic metabolic conditions (e.g. CVD)
  • Renal impairment (creatinine clearance <60 mL/min)
  • Uncontrolled hypothyroidism
  • Pregnant, breastfeeding, or postmenopausal females
  • Past (<6 year) or present use of nicotine products
  • Use of cannabis products
  • Use of any other medications that may affect study outcomes (e.g. anti-depressants)
  • Participants who have had a number of CT scans in the course of the year
  • Participants following a vegan diet

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Plant-based pea/lupine protein supplementProtein supplement - Plant protein-
Animal-based whey protein supplementProtein supplement - Animal protein-
Primary Outcome Measures
NameTimeMethod
Substrate oxidationBaseline and at 12 weeks

Substrate oxidation will be measured in a fasted state by indirect calorimetry. Volume of oxygen and carbon dioxide and water vapor pressure will be taken into consideration to calculate the respiratory exchange ratio.

LipidomicsBaseline and at 12 weeks

Lipidomics will be measured by mass spectrometry.

Adipocyte sizeBaseline and at 12 weeks

Regional adipocyte characteristics will be measured in vitro including adipocyte size,

Change in weightBaseline and at 12 weeks

Overall weight loss, kg

Change in overall body fat percentageBaseline and at 12 weeks

Body composition is measured by dual energy x-ray absorptiometry.

Regional subcutaneous adipose tissue immune cells ( number of cells per gram tissue, percentage of the stromal vascular compartment)Baseline and at 12 weeks

Changes in various adipose tissue immune cells including M1-like and M2-like macrophages, T helper cells, and cytotoxic T cells will be measured via flow cytometry.

Resting energy expenditureBaseline and at 12 weeks

Resting energy expenditure will be measured in a fasted state by indirect calorimetry. Volume of oxygen and carbon dioxide and water vapor pressure will be taken into consideration to calculate the resting energy expenditure.

Change in BMIBaseline and at 12 weeks

Height and weight will be combined to report BMI (kg/m\^2)

Change in fat massBaseline and at 12 weeks

Body composition is measured by dual energy x-ray absorptiometry.

Concentrations of Circulatory cytokines and adipokinesBaseline and at 12 weeks

Changes in cytokines and adipokines will be measured via ELISA. We will measure markers including interleukin 6, tumour necrosis factor a, leptin, and adiponectin.

Rate of pre-adipocyte proliferationBaseline and at 12 weeks

Regional adipose tissue pre-adipocyte proliferation rate will be measured in vitro

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

School of Health, Concordia University

🇨🇦

Montréal, Quebec, Canada

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