- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07456319
Sustainable Insect-based Protein Supplement in the Elderly: a Pilot Study (SIPSE)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Population aging and increasing environmental pressures on food systems underscore the need for sustainable dietary strategies that support healthy aging. Edible insects, such as Tenebrio molitor, provide high-quality protein with a substantially lower environmental footprint than conventional livestock and may represent a viable alternative protein source for older adults.
This pilot randomized, double-blind, parallel, controlled study was conducted in community-dwelling adults aged 60 years and older recruited from the Barcelona metropolitan area. Participants were randomly assigned to either an insect-based protein supplementation group or a control group. Both groups participated in an identical supervised physical activity program consisting of strength and resistance exercises performed three times per week over a 28-day intervention period.
The insect-based intervention consisted of three cookies per day, providing 35 g of Tenebrio molitor flour. Control cookies were wheat flour-based and matched for palatability and texture. Cookie consumption was supervised by a dietitian immediately after exercise sessions to ensure compliance. Participants were instructed to maintain their habitual diet and lifestyle throughout the study.
Primary outcomes included changes in conventional lipid profile parameters. Secondary outcomes comprised body weight, body composition, blood pressure, muscle strength and physical performance, glucose metabolism, hepatic enzymes, inflammatory biomarkers, advanced lipoprotein profiling, and plasma low-molecular-weight metabolites. Dietary intake was assessed using 3-day food records, and fasting blood samples were collected at baseline and post-intervention.
In addition, acceptability and organoleptic perception of the intervention products were evaluated using structured questionnaires, assessing taste, texture, appearance, and overall satisfaction. Gastrointestinal tolerance, including symptoms such as bloating, discomfort, and changes in bowel habits, was systematically recorded throughout the intervention. Participants' willingness to continue consuming the insect-based product after study completion was also assessed to explore feasibility and long-term adherence.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Barcelona
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Barcelona, Barcelona, Spain, 08018
- UOC
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 60 years
- Body mass index (BMI) between 18.5 and 30.0 kg/m²
- Mini-Mental State Examination (MMSE) score ≥ 16
- Independent in basic activities of daily living
- Mini Nutritional Assessment-Short Form (MNA-SF) score ≥ 8
- Ability to provide written informed consent
Exclusion Criteria:
- Food Neophobia Scale score > 4
- Chronic diseases affecting metabolism or nutritional status
- Dependency or severe functional impairment
- Current or past use of medications or supplements affecting body weight or metabolic function
- Excessive alcohol consumption
- History of eating disorders or psychiatric illness
- Known food allergies (e.g., crustacean allergy) or celiac disease
- Inability or unwillingness to comply with study procedures
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: INSECT
Participants consumed three Tenebrio molitor-enriched cookies per day (35 g insect flour/day) immediately after supervised exercise sessions, three times per week for 28 days.
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Participants received a protein suplement in the form of cookies based on edible insect flour.
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Placebo Comparator: CONTROL
Participants consumed three wheat flour-based control cookies per day immediately after supervised exercise sessions, three times per week for 28 days.
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Control placebo
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lipid profile
Time Frame: One month (baseline and after the intervention)
|
Changes in lipid profile (total cholesterol, LDL-C, HDL-C, triglycerides) and lipid particles (small, medium and large lipoproteins) Description: Changes in the lipid profile were assessed by measuring fasting plasma concentrations of total cholesterol, low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglycerides at baseline and after the intervention.
In addition, detailed lipoprotein particle profiling was performed to quantify the concentration and size distribution of lipoproteins, including small, medium, and large subclasses of LDL, HDL, and very-low-density lipoproteins (VLDL).
These measures allowed evaluation of both conventional lipid parameters and qualitative changes in lipoprotein particle composition associated with the intervention.
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One month (baseline and after the intervention)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Weight (Kg)
Time Frame: Baseline to 28 days
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Body weight will be measured in kilograms (kg) using a calibrated digital scale, with participants wearing light clothing and no shoes.
The change in body weight will be calculated as the difference between baseline and Day 28 measurements
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Baseline to 28 days
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Change in blood pressure (mmHg) .
Time Frame: Baseline to 28 days
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Changes in systolic and diastolic blood pressure will be assessed to evaluate the cardiovascular response to the dietary intervention throughout the study period.
Blood pressure will be measured in millimeters of mercury (mmHg) at baseline and at Day 28, using a calibrated sphygmomanometer.
Changes from baseline to Day 28 will be calculated for both systolic and diastolic values.
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Baseline to 28 days
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Change in Handgrip Strength (kg)
Time Frame: Baseline to 28 days
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Handgrip strength will be measured in kilograms (kg) using a calibrated handheld dynamometer under standardized conditions.
The outcome will be expressed as the maximum value obtained from repeated trials of the dominant hand.
The change in handgrip strength will be calculated as the difference between baseline and Day 28 measurements.
Higher values indicate greater muscle strength.
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Baseline to 28 days
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Change in glucose (mg/dL).
Time Frame: Baseline to 28 days
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Changes in fasting blood glucose will be measured in milligrams per deciliter (mg/dL) to determine changes in glycemic control associated with the dietary intervention.
Blood glucose concentrations will be measured at baseline and at Day 28, and changes from baseline to Day 28 will be calculated.
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Baseline to 28 days
|
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Change in hepatic enzymes (ALT, AST, GGT)
Time Frame: Baseline to 28 days
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Serum hepatic enzymes (ALT, AST, and GGT) will be analyzed as markers of liver function and to explore potential effects of the intervention on hepatic metabolic health.
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Baseline to 28 days
|
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Change in inflammatory biomarkers
Time Frame: Baseline to 28 days
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Circulating inflammatory biomarkers will be measured to evaluate changes in systemic inflammation in response to the intervention
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Baseline to 28 days
|
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Change in plasma low molecular weight metabolite
Time Frame: Baseline to 28 days
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Plasma low molecular weight metabolites will be analyzed using metabolomic approaches to characterize metabolic changes associated with the intervention.
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Baseline to 28 days
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Change in plasma and red blood cells fatty acids
Time Frame: Baseline to 28 days
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Fatty acid composition in plasma and red blood cells will be assessed to evaluate changes in lipid metabolism and fatty acid status following the intervention.
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Baseline to 28 days
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Changes in Energy Intake (kcal/day)
Time Frame: Frame: Baseline to 28 days
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Dietary intake will be assessed using 3-day food records collected at baseline and during the last week of the intervention.
Mean daily energy intake will be calculated and expressed in kilocalories per day (kcal/day) using EasyDiet software.
The change in energy intake will be calculated as the difference between baseline and Day 28 values.
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Frame: Baseline to 28 days
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Changes in Dietary Carbon Footprint (kg CO₂-eq/day)
Time Frame: Baseline to 28 days
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Dietary carbon footprint (kg CO₂-equivalents/day) will be estimated by linking reported food intake to a validated life cycle assessment database (Poore & Nemecek (via OWID) and WFLDB - World Food LCA Databas) Changes from baseline to the last week of intervention will be calculated.
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Baseline to 28 days
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Change in Body Mass Index (kg/m²)
Time Frame: Baseline to Day 28
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Body mass index (BMI) will be calculated as weight in kilograms divided by height in meters squared (kg/m²).
Height will be measured at baseline using a calibrated digital scale.
Changes in BMI will be calculated as the difference between baseline and Day 28 values.
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Baseline to Day 28
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Change in Body Fat Percentage (%)
Time Frame: Baseline to Day 28
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Body fat percentage (%) will be assessed using bioelectrical impedance analysis (BIA) under standardized conditions.
The change in body fat percentage will be calculated as the difference between baseline and Day 28 measurements.
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Baseline to Day 28
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Change in Lean Mass Percentage (%)
Time Frame: Baseline to Day 28
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Lean mass percentage (%) will be assessed using bioelectrical impedance analysis (BIA) under standardized conditions.
The change in lean mass percentage will be calculated as the difference between baseline and Day 28 measurements.
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Baseline to Day 28
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Change in Protein Intake (g/day)
Time Frame: Baseline to Day 28
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Dietary intake will be assessed using 3-day food records collected at baseline and during the last week of the intervention.
Mean daily protein intake will be calculated and expressed in grams per day (g/day) using EasyDiet software.
The change in protein intake will be calculated as the difference between baseline and Day 28 values.
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Baseline to Day 28
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Change in Vivifrail Physical Performance Battery Total Score (points)
Time Frame: Baseline to Day 28
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Changes in physical performance will be assessed using the Vivifrail Physical Performance Battery (VPPB), a standardized functional assessment that evaluates lower-limb strength, balance, gait speed, and functional capacity in older adults. The total score ranges from 0 to 12 points, with higher scores indicating better physical performance. The primary outcome will be the change in the total VPPB score, calculated as the difference between baseline and Day 28 measurements. [Time Frame: Baseline to Day 28]. |
Baseline to Day 28
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Ros-Baro M, Puig MC, Chiva-Blanch G, Diaz-Rizzolo DA, Martinez AA, Rafart MJ, Chiriac I, Rogel MB, Cunill MP, Casas-Agustench P, Bach-Faig A. Enrichment of Pasteurized Dairy Product and Brownie With Edible Insect (Tenebrio molitor) to Analyze Acceptance Using Check-All-That-Apply Methodology. Food Sci Nutr. 2025 Oct 30;13(11):e70925. doi: 10.1002/fsn3.70925. eCollection 2025 Nov.
- Ros-Baro M, Casas-Agustench P, Diaz-Rizzolo DA, Batlle-Bayer L, Adria-Acosta F, Aguilar-Martinez A, Medina FX, Pujola M, Bach-Faig A. Edible Insect Consumption for Human and Planetary Health: A Systematic Review. Int J Environ Res Public Health. 2022 Sep 15;19(18):11653. doi: 10.3390/ijerph191811653.
- Ros-Baro M, Sanchez-Socarras V, Santos-Pages M, Bach-Faig A, Aguilar-Martinez A. Consumers' Acceptability and Perception of Edible Insects as an Emerging Protein Source. Int J Environ Res Public Health. 2022 Nov 26;19(23):15756. doi: 10.3390/ijerph192315756.
- Ishara J, Ekaette I, Matendo R, Vandenberg G, Niassy S, Katcho K, Kinyuru J. Potential health benefits of insect bioactive metabolites and consumer attitudes towards edible insects. NPJ Sci Food. 2025 Sep 26;9(1):195. doi: 10.1038/s41538-025-00549-x.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RA2024
- RA2024. (Other Identifier: UNIVERSITAT OBERTA DE CATALUNYA (UOC))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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