SUSTAINA Study: Effects of Sustainable Diet and Therapeutic Exercise on Health in Young Athletes (SUSTAINA)

April 27, 2026 updated by: Prof. Dr. Alejandro Martínez-Rodríguez, University of Alicante

Research and Development of New Sustainable Dietary and Nutritional Programs and Therapeutic Exercise for the Prevention of Metabolic and Musculoskeletal Disorders

The SUSTAINA study aims to evaluate the effects of sustainable dietary programs combined with individualized therapeutic exercise on metabolic health, body composition, and musculoskeletal function in young athletes. Participants will be randomly assigned to different intervention groups receiving tailored exercise training and nutritional guidance based on Mediterranean diet principles. The study will assess physiological, anthropometric, and functional outcomes to identify effective strategies for preventing metabolic and musculoskeletal disorders.

Study Overview

Detailed Description

This study is a randomized controlled trial designed to investigate the impact of combined dietary and exercise interventions on health outcomes in young athletes. Participants will be allocated into different groups, including a control group and intervention groups receiving structured therapeutic exercise programs and personalized nutritional strategies based on sustainable Mediterranean diet principles.

Measurements will include body composition, metabolic parameters, physical performance, and musculoskeletal function. The intervention is expected to provide evidence-based strategies to prevent metabolic and musculoskeletal disorders in physically active populations.

Study Type

Interventional

Enrollment (Actual)

70

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

    • Alicante
      • Elche, Alicante, Spain, 03202
        • European Institute Of Exercise and Health

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 14 and 25 years
  • Regular participation in organized physical activity (≥4 days per week)
  • Healthy individuals without diagnosed metabolic or musculoskeletal disorders
  • Ability to participate in physical exercise programs
  • Written informed consent provided by the participant or legal guardian (for minors)

Exclusion Criteria:

  • Presence of diagnosed metabolic disease (e.g., diabetes, cardiovascular disease)
  • Musculoskeletal injury or condition that prevents participation in exercise
  • Any medical condition contraindicating physical activity
  • Use of medication or treatment that may affect metabolic or physical performance outcomes
  • Failure to comply with study procedures or intervention protocols

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Arm 1: Control Group
Nutritional intervention only (no structured exercise). Participants receive a personalized dietary intervention based on Mediterranean diet principles, without participation in a structured exercise program.
Personalized dietary program based on sustainable Mediterranean diet principles, adapted to individual energy and nutritional requirements.
Experimental: Arm 2: Traditional resistance training (hypertrophy) + nutritional intervention
Participants perform a hypertrophy-focused resistance training program combined with a personalized dietary intervention.
Personalized dietary program based on sustainable Mediterranean diet principles, adapted to individual energy and nutritional requirements.
Traditional resistance training program including hypertrophy and strength-based exercises using guided machines and free weights.
Experimental: Arm 3: Explosive strength training + nutritional intervention
Participants perform an explosive strength training program combined with a personalized dietary intervention.
Personalized dietary program based on sustainable Mediterranean diet principles, adapted to individual energy and nutritional requirements.
High-intensity strength training focused on explosive movements using free weights.
Experimental: Arm 4: Functional training + nutritional intervention
Participants perform a functional training program using alternative materials combined with a personalized dietary intervention.
Personalized dietary program based on sustainable Mediterranean diet principles, adapted to individual energy and nutritional requirements.
Exercise program based on functional movements using alternative training materials.
Experimental: Arm 5: Isoinertial training + nutritional intervention
Participants perform an isoinertial resistance training program combined with a personalized dietary intervention.
Personalized dietary program based on sustainable Mediterranean diet principles, adapted to individual energy and nutritional requirements.
Resistance training program using isoinertial devices with an emphasis on eccentric load.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in fat mass
Time Frame: Baseline to 9 months
Assessment of fat mass using dual-energy X-ray absorptiometry (DXA) and bioelectrical impedance analysis.
Baseline to 9 months
Change in lean body mass
Time Frame: Baseline to 9 months
Assessment of lean body mass using dual-energy X-ray absorptiometry (DXA) and bioelectrical impedance analysis.
Baseline to 9 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in blood glucose levels
Time Frame: Baseline to 9 months
Measurement of blood glucose levels using a portable biochemical analyzer.
Baseline to 9 months
Change in triglyceride levels
Time Frame: Baseline to 9 months
Assessment of triglyceride levels using a portable biochemical analyzer.
Baseline to 9 months
Change in bone mineral content
Time Frame: Baseline to 9 months
Assessment of bone mineral content using dual-energy X-ray absorptiometry (DXA).
Baseline to 9 months
Change in total cholesterol levels
Time Frame: Baseline to 9 months
Assessment of total cholesterol levels using a portable biochemical analyzer.
Baseline to 9 months
Change in handgrip strength
Time Frame: Baseline and 9 months
Assessment of upper body isometric strength using a handgrip dynamometer. Measured in kilograms (kg)
Baseline and 9 months
Change in lower body strength (countermovement jump height)
Time Frame: Baseline and 9 months
Assessment of lower body strength using countermovement jump (CMJ) height measured with a contact platform (cm).
Baseline and 9 months
Change in sprint performance
Time Frame: Baseline and 9 months
Assessment of sprint performance using 10-30 meter sprint tests measured with photocell timing systems. Measured in seconds (s)
Baseline and 9 months
Change in endurance capacity (Yo-Yo Intermittent Recovery Test Level 1)
Time Frame: Baseline and 9 months
Assessment of endurance capacity using the Yo-Yo Intermittent Recovery Test Level 1, expressed as total distance covered (meters).
Baseline and 9 months
Change in functional movement (Functional Movement Screen score)
Time Frame: Baseline and 9 months
Assessment of functional movement using the Functional Movement Screen (FMS), scored from 0 to 21 points, where higher scores indicate better movement quality and lower injury risk.
Baseline and 9 months
Change in joint range of motion
Time Frame: Baseline and 9 months
Assessment of joint range of motion using goniometric measurements.
Baseline and 9 months
Change in urine specific gravity
Time Frame: Baseline and 9 months
Assessment of hydration status using urine specific gravity measured by refractometry.
Baseline and 9 months
Change in hydration status (urine color scale)
Time Frame: Baseline and 9 months
Assessment of hydration status using a validated urine color scale ranging from 1 to 8, where lower values indicate better hydration status and higher values indicate dehydration.
Baseline and 9 months
Change in blood pressure
Time Frame: Baseline and 9 months
Measurement of systolic and diastolic blood pressure using a digital sphygmomanometer.
Baseline and 9 months
Change in basal metabolic rate
Time Frame: Baseline and 9 months
Assessment of basal metabolic rate using indirect calorimetry.
Baseline and 9 months

Collaborators and Investigators

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

January 1, 2026

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

September 30, 2026

Study Registration Dates

First Submitted

April 20, 2026

First Submitted That Met QC Criteria

April 27, 2026

First Posted (Actual)

May 5, 2026

Study Record Updates

Last Update Posted (Actual)

May 5, 2026

Last Update Submitted That Met QC Criteria

April 27, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UA-2026-02-19_3

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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