Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07165548

Impact of Satiating Compounds and Hypocaloric Diet on Weight, Cardiometabolic and Osteoarticular Health in Obesity

The main objective of this intervention study is to evaluate the effect of satiating protein and/or fiber bar consumption on weight loss and other osteoarticular and cardiometabolic parameters related to excess weight in subjects with overweight or obesity.

To achieve this objective, volunteers will be instructed to consume three bars per day as part of a hypocaloric diet, in accordance with healthy nutritional guidelines, over a 12-week period.

The main questions to answer are:

* Does the regular consumption of these protein and/or fiber bars help to lose weight? * Does the regular consumption of these protein and/or fiber bars help to improve the osteoarticular health? * Does the regular consumption of these protein and/or fiber bars help to improve the cardiometabolic health?

The specific objectives are focused on evaluating the effects of the intervention on the following parameters:

* Weight and body composition. * Knee joint range of motion. * Blood biomarkers related to collagen degradation and synthesis, associated with osteoarticular health. * Glycemic and lipid profiles, blood pressure, and biomarkers of kidney, liver, cardiovascular, and inflammatory health. * Changes in joint discomfort (improvement or worsening). * Adherence to the assigned intervention, including both dietary compliance and intake of the study-provided supplement. * Satiety-related variables assessed using a visual analog scale (VAS). * Urinary hydroxyproline and stool samples for metagenomic analysis. * Gastrointestinal health, mental health, quality of life, and physical activity level assessed through validated questionnaires.

Target sample size is 144 subjects and participants will be allocated in four different groups:

* Group 1 (n=36): hypocaloric diet + protein and fiber supplement. * Group 2 (n=36): hypocaloric diet + protein and fiber supplement. * Group 3 (n=36): hypocaloric diet + fiber supplement. * Group 4 "Placebo group" (n=36): hypocaloric diet + placebo supplement. Participants will attend the nutritional intervention unit at weeks 1, 8, and 12. A follow-up phone call will be conducted at week 4.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Obesity Body Weight Body Weight Changes Nutrition Disorders Nutritional and Metabolic Diseases Overnutrition Overweight Pathological Conditions, Signs and Symptoms Signs and Symptoms Weight Loss

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Nutrition Research

Pamplona, Navarre, 31008, Spain

Location status: Recruiting

Location contact

María Ángeles Zulet, PhD

CONTACT

[email protected]

948425600 ext. 806317

About this study

Volunteers expressing interest in the study will undergo an initial eligibility assessment, either via telephone interview or by completing an online screening form (Google Form), to verify compliance with the primary inclusion criteria. Candidates meeting these criteria will be invited to attend an information and screening visit, during which the study procedures will be explained in detail and any questions addressed. Individuals who agree to participate will provide written informed consent and will be randomly allocated to one of the four intervention groups. All necessary study materials will be provided at this stage.

Participants will attend three scheduled clinical investigation visits: baseline (day 0), mid-intervention (week 8), and post-intervention (week 12). At each visit, anthropometric and body composition measurements will be performed, and blood pressure will be recorded. Biological samples, including blood, urine, and stool, will be collected. In addition, data regarding dietary intake, physical activity levels, sleep patterns, and gastrointestinal symptoms will be obtained through validated questionnaires.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Volunteers of both sexes between the ages of 18 and 65 years old.
  • Volunteers with grade II overweight or obesity (BMI: 27.0-39.9 kg/m2).
  • Physical examination and vital signs are normal or clinically irrelevant to the study.
  • Volunteers receiving pharmacological treatment may be included if the dosage has remained stable for at least three months prior to study initiation.
  • Individuals undergoing treatment for diabetes will be excluded.
  • Participants must be capable of understanding the study requirements, willing to provide written informed consent, and able to comply with all study procedures and timelines.
  • Body weight must have remained stable (±5%) during the three months preceding study initiation.

Exclusion criteria

  • Presence of significant functional or structural abnormalities of the digestive system, including but not limited to congenital malformations, angiodysplasia, active peptic ulcer disease, chronic inflammatory or malabsorption disorders, hiatal hernia, or chronic gastroesophageal reflux.
  • High alcohol consumption, defined as >14 units per week for women and >20 units per week for men.
  • Pregnancy or lactation at the time of screening.
  • History of surgical procedures resulting in permanent alterations of the digestive system (e.g., gastroduodenostomy) or joint replacement surgery (hip or knee).
  • Diagnosis of arthritis.
  • History of any liver disease, with the exception of non-alcoholic fatty liver disease.
  • Diagnosis of any type of cancer, current cancer treatment, or history of cancer treatment within the past five years.
  • Known allergy or hypersensitivity to any component of the investigational product or to any food that could interfere with study participation and follow-up.
  • Presence of cognitive and/or psychological impairment that could affect study compliance.
  • Anticipated poor adherence or, in the opinion of the investigator, inability to comply with study procedures.
  • Engagement in night-shift work.
  • Current use of dietary supplements that may interfere with study outcomes (e.g., nutraceuticals containing compounds with potential weight loss effects).
  • Ongoing treatment for weight loss or diabetes.

Treatment and study plan

Experimental Bar (Formulation 1) + Hypocaloric diet (10% energy restriction)

Dietary Supplement

Participants will consume three satiating compound-enriched bars (formulation 1) daily, 30 minutes before breakfast, lunch, and dinner, as part of a 10% energy-restricted hypocaloric diet for 12 weeks.

Experimental Bar (Formulation 2) + Hypocaloric diet (10% energy restriction)

Dietary Supplement

Participants will consume three satiating compound-enriched bars (formulation 2) daily, 30 minutes before breakfast, lunch, and dinner, as part of a 10% energy-restricted hypocaloric diet for 12 weeks.

Experimental Bar (Formulation 3) + Hypocaloric diet (10% energy restriction)

Dietary Supplement

Participants will consume three satiating compound-enriched bars (formulation 3) daily, 30 minutes before breakfast, lunch, and dinner, as part of a 10% energy-restricted hypocaloric diet for 12 weeks.

Placebo Bar + Hypocaloric diet (10% energy restriction)

Dietary Supplement

Participants will consume three placebo bars daily, 30 minutes before breakfast, lunch, and dinner, as part of a 10% energy-restricted hypocaloric diet for 12 weeks.

Primary outcomes

  1. Body weight

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Weight of participants will be measured by bioimpedance an densitometry and reported in kg

Secondary outcomes

  1. Height

    Time frame: Clinical Investigation Day 1

    Height of participants will be measured by stadiometer and reported in cm.

  2. Body mass index

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Body mass index will be calculated as follows: weight (kilograms)/ height (m)2

  3. Waist circumference

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Waist circumference of participants in fasting condition will be analyzed by measuring tape and reported in centimeters.

  4. Hip circumference

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Hip circumference of participants in fasting condition will be analyzed by measuring tape and reported in centimeters.

  5. Neck circumference

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Neck circumference of participants in fasting condition will be analyzed by measuring tape and reported in centimeters.

  6. Body fat mass

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Body fat of participants will be analyzed by bioimpedance and densitometry and reported in percentage and kilograms.

  7. Body lean mass

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Body lean mass of participants will be analyzed by bioimpedance and densitometry and reported in kilograms.

  8. Body muscle mass

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Body muscle mass of participants will be analyzed by bioimpedance and densitometry and reported in kilograms.

  9. Fat free mass

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Fat free mass of participants will be analyzed by densitometry and reported in kilograms.

  10. Visceral fat

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Visceral fat of participants will be measured by bioimpedance an densitometry and reported in g.

  11. Body water mass

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Body water mass of participants will be analyzed by bioimpedance and densitometry and reported in kilograms and percentage.

  12. Body bone mass

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Body bone mass Body bone mass of participants will be analyzed by bioimpedance and densitometry and reported in kilograms.

  13. Systolic blood pressure

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Systolic blood pressure of participants in fasting condition will be analyzed by electronic tensiometer and reported in mmHg

  14. Diastolic blood pressure

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Diastolic blood pressure of participants in fasting condition will be analyzed by electronic tensiometer and reported in mmHg

  15. Heart rate

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Heart rate of participants in fasting condition will be analyzed by electronic tensiometer and reported in pulses/min.

  16. Total bone mineral density

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Total bone mineral density of participants will be analyzed by densitometry and reported in g/cm2.

  17. Bone mineral density L1-L4

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Bone mineral density L1-L4 of participants will be analyzed by densitometry and reported in g/cm2.

  18. Total bone mineral density femur

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Total bone mineral density femur of participants will be analyzed by densitometry and reported in g/cm2.

  19. Bone mineral density femur neck

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Bone mineral density femur neck of participants will be analyzed by densitometry and reported in g/cm2.

  20. Knee articular range

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Knee articular range of participants will be measured using a goniometer and performing the chair test.

  21. Grip strength

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Grip strength of participants will be measured using a manual dynamometer and reported in kg.

  22. Level of hunger

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2

    Hunger of participants will be analyzed by Hunger-Satiety Visual Analogue Scale (VAS). The minimum value of the scale is 0 mm and the maximum value is 100 mm. A reduction in hunger scale means better outcome.

  23. Level of fullness

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2

    Fullness of participants will be analyzed by Hunger-Satiety Visual Analogue Scale. The minimum value of the scale is 0 mm and the maximum value 100 mm. An incrementation in fullness scale means better outcome.

  24. Level of satisfaction

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2

    Satisfaction sensation of participants will be analyzed by Hunger-Satiety Visual Analogue Scale. The minimum value of the scale is 0 mm and the maximum value 100 mm. An incrementation in satisfaction scale means better outcome.

  25. Want to eat something else

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2

    Want to eat something else sensation of participants will be analyzed by Hunger-Satiety Visual Analogue Scale. The minimum value of the scale is 0 mm and the maximum value 100 mm. A reduction in want to eat something else scale means better outcome.

  26. Thirst

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2

    Thirst sensation of participants will be analyzed by Hunger-Satiety Visual Analogue Scale. The minimum value of the scale is 0 mm and the maximum value 100 mm.

  27. Life quality

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Life quality of participants will be evaluated by SF-36 questionnaire (36-Item Short Form Survey).

  28. Depression

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Depression will be evaluated using the Beck Depression Inventory-II (BDI-II), a 21-item self-report questionnaire. Total scores range from 0 to 63, with higher scores indicating greater severity of depressive symptoms.

  29. Anxiety

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Anxiety will be evaluated using the State-Trait Anxiety Inventory (STAI), a 40-item self-report questionnaire that includes two subscales: State Anxiety (20 items) and Trait Anxiety (20 items). Each subscale yields scores ranging from 20 to 80, with higher scores indicating greater levels of anxiety.

  30. Osteoarticular health

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Osteoarticular health of participants will be measured using the Western Ontario and McMaster Universities Arthritis Index (WOMAC), a 24-item self-report questionnaire that assesses pain (range 0-20), stiffness (range 0-8), and physical function (range 0-68). The total score ranges from 0 to 96, with higher scores indicating worse osteoarticular symptoms and functional impairment.

  31. Physical activity

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Physical activity will be evaluated using the Physical Activity Questionnaire of the Seguimiento Universidad de Navarra (SUN) cohort, which estimates total physical activity expressed in Metabolic Equivalent of Task hours per week (MET-h/week). Higher values indicate greater levels of physical activity. Participants can also be classified into categories of low, moderate, or high physical activity according to standardized SUN cohort scoring procedures.

  32. Gastrointestinal symptoms

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Gastrointestinal symptoms will be registrated through Gastrointestinal Symptoms Rating Scale questionnaire, which is a questionnaire of 15 items. The questionnaire has a seven-point graded likert-type scale, where 1 represents absence of troublesome symptoms and 7 represents very troublesome symptoms.

  33. Glucose concentration

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood glucose levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in mg/dL.

  34. Insulin concentration

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood insulin concentration will be analyzed after an overnight fast by ELISA kit and reported in μUI/ml.

  35. HOMA index (Homeostatic Model Assessment Index)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    HOMA index will be calculated as follows: HOMA-IR (Homeostatic Model Assessment for Insulin Resistance)= [fasting glucose (mmol/L) x fasting insulin (μU/ml)] / 22.5.

  36. Total cholesterol

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood total cholesterol levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in mg/dL

  37. HDL cholesterol

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood HDL cholesterol levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in mg/dL

  38. LDL cholesterol

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    LDL cholesterol levels of participants in fasting condition will be analyzed by Friedewald formula and reported in mg/dL.

  39. Triglyceride concentration

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Triglyceride levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in mg/dL.

  40. Alanine aminotransferase

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Alanine aminotransferase levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in UI/L.

  41. Aspartate aminotransferase

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Aspartate aminotransferase levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in UI/L.

  42. Gamma-glutamyl transferase

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Gamma-glutamyl transferase levels of participants in fasting condition will be analyzed by biochemical autoanalyzer and reported in UI/L.

  43. Fatty liver Index (FLI)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Fatty liver Index will be calculated as follows FLI = (e 0.953 × ln (triglycerides) + 0.139 × BMI + 0.718 × ln (ggt) + 0.053 × waist circumference - 15.745)/ (1 + e 0.953 × ln (triglycerides) + 0.139 × BMI + 0.718 × ln (ggt) + 0.053 × waist circumference - 15.745) × 100

  44. Fructosamine concentration

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood fructosamine concentration will be analyzed after an overnight fast by ELISA kit and reported in µg/L.

  45. Leptine

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood leptine concentration will be analyzed after an overnight fast by ELISA kit and reported in ng/ml

  46. Adiponectin

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood adiponectin concentration will be analyzed after an overnight fast by ELISA kit and reported in ng/ml.

  47. Homocysteine

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood homocysteine concentration will be analyzed after an overnight fast by biochemical autoanalyzer and reported in μmol/L.

  48. MCP1 (Monocyte Chemoattractant Protein-1)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood MCP1 concentration will be analyzed after an overnight fast by ELISA kit and reported in pg/ml.

  49. TNF-alpha (tumor necrosis factor alpha)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    TNF-alpha will be analyzed after an overnight fast by ELISA kit and reported in pg/ml.

  50. Interleukin 6 (IL6)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood IL6 concentration will be analyzed after an overnight fast by ELISA kit and reported in pg/ml.

  51. C Reactive protein (CRP)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Blood CRP concentration will be analyzed after an overnight fast by ELISA kit and reported in mg/L

  52. Blood glycated hemoglobin

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Fasting blood glycated hemoglobin will be reported in percentage.

  53. Plasma CTX-II levels (C-terminal telopeptide of type II collagen)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Plasma CTX-II levels will be analyzed after an overnight fast by ELISA kit and reported in ng/ml

  54. Plasma C2C levels (Cartilage Collagen Neoepitope)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Plasma C2C levels will be analyzed after an overnight fast by ELISA kit and reported in ng/ml.

  55. Plasma CP2 levels (type II procollagen carboxy-propeptide)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3.

    Plasma CP2 levels will be analyzed after an overnight fast by ELISA kit and reported in ng/ml.

  56. Albumin concentration

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Albumin levels of participants in fasting condition will be analyzed in urine by biochemical autoanalyzer and reported in mg/dl.

  57. Creatinine concentration

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Creatinine levels of participants in fasting condition will be analyzed in urine by biochemical autoanalyzer and reported in mg/dl.

  58. Hydroxyproline

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Urine hydroxyproline concentration will be analyzed after an overnight fast by colorimetry technique and reported in mg/ml.

  59. Blood untargeted metabolomics

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Untargeted metabolites will be expressed and analyzed in plasma and serum according to their intensity measured in arbitrary units (UA), which carries a direct relation with its concentration.

  60. Urine untargeted metabolomics

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Untargeted metabolomics will be expressed and analyzed in urine according to their intensity measured in arbitrary units (UA), which carries a direct relation with its concentration.

  61. Lipidomic

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Lipidomic will be expressed and analyzed in plasma and serum according to their intensity measured in arbitrary units (UA), which carries a direct relation with its concentration.

  62. Dietary Intake (Energy and Nutrients)

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Dietary intake will be assessed using the Food Frequency Questionnaire (FFQ). Outcomes will include energy intake (kcal/day), macronutrient intake (g/day), and micronutrient intake (mg/day or µg/day).

  63. Mediterranean Diet Adherence

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2 and Clinical Investigation Day 3

    Adherence to the Mediterranean dietary pattern will be evaluated using the Mediterranean Diet Adherence Questionnaire, with scores ranging from 0 to 14 points. Higher scores indicate greater adherence to the Mediterranean diet.

  64. Snacking frequency

    Time frame: Clinical Investigation Day 1, Clinical Investigation Day 2, and Clinical Investigation Day 3

    Snacking behavior will be recorded using a daily snacking record. Results will be expressed as number of snacks per day.

  65. Adherence to bars consumption

    Time frame: Clinical Investigation Day 2 and Clinical Investigation Day 3

    Adherence will be assessed using the bars consumption record form.

  66. Acceptance of bars

    Time frame: Clinical Investigation Day 3

    Acceptance will be assessed using the acceptance consumption record form.

Study contacts

Contact information is provided by the study sponsor or research team.

Fermín Milagro, PhD

CONTACT

[email protected]

+34948425600 ext. 806553

María Ángeles Zulet, PhD

CONTACT

[email protected]

+34948425600 ext. 806317

Sponsors and collaborators

Lead sponsor

Clinica Universidad de Navarra, Universidad de Navarra

Other

Registry information

Official study title

Evaluation of the Effect of Supplementation With Satiating Compounds Integrated Into a Hypocaloric Diet on Weight and Cardiometabolic and Osteoarticular Health in Overweight/Obese Subjects

Acronym: COGLUBOCO

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 10, 2025
Registry last updated
Sep 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.