Sustainable Insect-based Protein Supplement in the Elderly: a Pilot Study (SIPSE)

March 5, 2026 updated by: Gemma Chiva-Blanch, PhD, Universitat Oberta de Catalunya
This pilot randomized, double-blind, controlled trial evaluated the effects of a Tenebrio molitor-enriched protein biscuit combined with a structured physical activity program on cardiometabolic health in older adults. Participants aged 65 years and older were assigned to receive either insect-based or control biscuits following supervised exercise sessions for 28 days. Primary outcomes focused on changes in lipid profile, while secondary outcomes included anthropometric measures, body composition, blood pressure, physical function, glucose metabolism, hepatic function and inflammatory biomarkers.

Study Overview

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

Interventional

Enrollment (Actual)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Barcelona
      • Barcelona, Barcelona, Spain, 08018
        • UOC

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
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.
Participants received a protein suplement in the form of cookies based on edible insect flour.
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.
Control placebo

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.
One month (baseline and after the intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Weight (Kg)
Time Frame: Baseline to 28 days
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
Baseline to 28 days
Change in blood pressure (mmHg) .
Time Frame: Baseline to 28 days
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.
Baseline to 28 days
Change in Handgrip Strength (kg)
Time Frame: Baseline to 28 days
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.
Baseline to 28 days
Change in glucose (mg/dL).
Time Frame: Baseline to 28 days
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.
Baseline to 28 days
Change in hepatic enzymes (ALT, AST, GGT)
Time Frame: Baseline to 28 days
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.
Baseline to 28 days
Change in inflammatory biomarkers
Time Frame: Baseline to 28 days
Circulating inflammatory biomarkers will be measured to evaluate changes in systemic inflammation in response to the intervention
Baseline to 28 days
Change in plasma low molecular weight metabolite
Time Frame: Baseline to 28 days
Plasma low molecular weight metabolites will be analyzed using metabolomic approaches to characterize metabolic changes associated with the intervention.
Baseline to 28 days
Change in plasma and red blood cells fatty acids
Time Frame: Baseline to 28 days
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.
Baseline to 28 days
Changes in Energy Intake (kcal/day)
Time Frame: Frame: Baseline to 28 days
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.
Frame: Baseline to 28 days
Changes in Dietary Carbon Footprint (kg CO₂-eq/day)
Time Frame: Baseline to 28 days
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.
Baseline to 28 days
Change in Body Mass Index (kg/m²)
Time Frame: Baseline to Day 28
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.
Baseline to Day 28
Change in Body Fat Percentage (%)
Time Frame: Baseline to Day 28
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.
Baseline to Day 28
Change in Lean Mass Percentage (%)
Time Frame: Baseline to Day 28
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.
Baseline to Day 28
Change in Protein Intake (g/day)
Time Frame: Baseline to Day 28
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.
Baseline to Day 28
Change in Vivifrail Physical Performance Battery Total Score (points)
Time Frame: Baseline to Day 28

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2024

Primary Completion (Actual)

December 22, 2024

Study Completion (Actual)

December 22, 2024

Study Registration Dates

First Submitted

February 11, 2026

First Submitted That Met QC Criteria

March 2, 2026

First Posted (Actual)

March 6, 2026

Study Record Updates

Last Update Posted (Actual)

March 9, 2026

Last Update Submitted That Met QC Criteria

March 5, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

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

No

Studies a U.S. FDA-regulated device product

No

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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