Prevention of Energy Deficit Syndrome in Female Athletes. Molecular Mechanisms Associated With Malnutrition.

Sponsor
University of Alicante (Other)
Overall Status
Recruiting
CT.gov ID
NCT05567211
Collaborator
(none)
50
1
4
21.9
2.3

Study Details

Study Description

Brief Summary

Energy Deficit Syndrome (RED-S) is the impairment of physiological functioning caused by relative energy deficiency and includes impaired metabolic rate, menstrual, endocrine, hematological, immunological, gastrointestinal, bone, psychological, developmental and cardiovascular function. Eighty-seven percent of athletes show at least one symptom related to RED-S, with a higher prevalence in women. Treatment of RED-S preferably involves a multidisciplinary team of health professionals to address the complex interaction of nutrition, training, body image and performance. The main objective is to prevent energy deficit syndrome in female athletes in the province of Alicante through different training and diet protocols using a virtual platform. A 12-week single-blind randomized clinical trial with an intervention period and a control period (RCT) is proposed. The sports federations of the most representative practices in the province of Alicante will be selected by randomized sampling. The female athletes will be randomly divided into 4 groups (control group; control group with free use of the virtual platform; intervention group with Mediterranean diet and physical exercise planning; intervention group with red fruits and physical exercise planning).

Condition or Disease Intervention/Treatment Phase
  • Other: Free use of the virtual platform.
  • Other: Personalized nutritional planning based on the Mediterranean diet + physical exercise + use of mobile application.
  • Other: Personalized nutritional planning with an extra intake of berries + physical exercise + use of mobile application.
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
Prevention of Energy Deficit Syndrome in Female Athletes. Molecular Mechanisms Associated With Malnutrition: Oxidative Stress and Other Physiological, Physical and Psychological Alterations.
Actual Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Sep 30, 2023
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

Will receive basic recommendations from the World Health Organization on healthy eating and physical activity.

Placebo Comparator: Control group with free use of the virtual platform

The athletes, in addition to the recommendations indicated in the previous point, will have access to the virtual platform designed to voluntarily record the parameters they consider appropriate.

Other: Free use of the virtual platform.
Access to the virtual platform + general healthy eating and physical activity recommendations. The platform will allow the registration of all the evolution, monitoring of nutritional and sports patterns (with activity bracelet), as well as oxidative stress, hydration, menstrual phase and mood.

Active Comparator: Intervention group with Mediterranean diet and physical exercise planning

They will receive nutritional plans adapted to their energy expenditure and based on Mediterranean diet. The physical exercise intervention will be based on 3 weekly sessions of 50 minutes of combined resistance and strength, deferred.

Other: Personalized nutritional planning based on the Mediterranean diet + physical exercise + use of mobile application.
Access to the virtual platform + nutritional planning based on the Mediterranean diet + physical activity. The platform will allow the registration of all the evolution, monitoring of nutritional and sports patterns (with activity bracelet), as well as oxidative stress, hydration, menstrual phase and mood.

Active Comparator: Intervention group with red berries and physical exercise planning

They will also receive personalized nutritional plans with a diet rich in antioxidants obtained from red berries and the same physical exercise intervention as in the Mediterranean diet intervention group.

Other: Personalized nutritional planning with an extra intake of berries + physical exercise + use of mobile application.
Access to the virtual platform + nutritional planning with an extra supply of antioxidants using red berries + physical activity. The platform will allow the registration of all the evolution, monitoring of nutritional and sports patterns (with activity bracelet), as well as oxidative stress, hydration, menstrual phase and mood.

Outcome Measures

Primary Outcome Measures

  1. Oxidative stress [12 weeks]

    Measurement of oxidative stress by pentane by exhaled air

  2. Weight [12 weeks]

    Weight evaluation using a digital scale

  3. Anthropometric assessment - Height [12 weeks]

    Restricted profile proposed by the International Society for the Development of Cineanthropometry.

  4. Fat mass [12 weeks]

    Through anthropometry. Restricted profile proposed by the International Society for the Development of Cineanthropometry. The Faulkner formula will be used.

  5. Muscular mass [12 weeks]

    Through anthropometry. Restricted profile proposed by the International Society for the Development of Cineanthropometry. Lee's formula will be used.

  6. Bone mass [12 weeks]

    Through anthropometry. Restricted profile proposed by the International Society for the Development of Cineanthropometry. The Rocha formula will be used.

  7. Hydratation [12 weeks]

    Urine density will be measured with Refractometer.

  8. Menstrual cycle [12 weeks]

    Using the Relative Energy Deficiency in Sport (RED-S) Clinical Assessment Tool (CAT) questionnaire. It is a clinical assessment tool for the evaluation of athletes / active individuals suspected of having relative energy deficiency and for guiding return to play decisions.

  9. Gastrointestinal symptoms [12 weeks]

    The questionnaire on irritable bowel syndrome and symptom management among endurance athletes will be used; https://pubmed.ncbi.nlm.nih.gov/30232638/

  10. Maximal oxygen uptake (VO2 max.) [12 weeks]

    In cycloergometer and cardiorespiratory fitness test monitored with electrocardiogram

  11. Blood pressure [12 weeks]

    Using an OMROM upper arm blood pressure monitor.

  12. Cholesterol in blood [12 weeks]

    Cholesterol by blood test

  13. Strength [12 weeks]

    All participants will perform a countermovement jump, using a contact platform. Higher values will mean better performance.

  14. Creatin-Kinase in blood [12 weeks]

    Creatin-Kinase by blood test (milligrams/deciliters). High values may be a sign of overtraining.

  15. Perception of quality of life [12 weeks]

    Using a Quality of Life Questionnaire (SF36). Quality of Life Questionnaire is a comprehensive questionnaire that covers various attributes of an individuals life. It covers a variety of demographic questions to get better quality data and information before analyzing the quality of life of an individual.The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability.

  16. Mood state [12 weeks]

    Profile of Mood State Questionnaire (POMS). The POMS questionnaire assesses six mood subscales: tension-anxiety, depression, anger-hostility, vigor, fatigue, and confusion. High vigor scores reflect a good mood or emotion, and low scores in the other subscales reflect a good mood or emotion.

  17. Eating behavior [12 weeks]

    Eating Behavior Questionnaire (EAT-26). It is used to identify the presence of "eating disorder risk" based on attitudes, feelings and behaviours related to eating. There are 26 self-report questions assessing general eating behaviour and five additional questions assessing risky behaviours. The total score (between 0 and 78) provides an overall risk score, where higher scores indicating greater risk of an eating disorder. Total scores 20 or above are considered to be in the clinical range.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • (a) exercise at least 3 days/week,

  • (b) not having any diagnosed chronic pathology or ailment that prevents physical exercise or following nutritional guidelines rich in antioxidants.

Exclusion Criteria:
  • All individuals taking medication that could affect the results of the study will be excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Alejandro Martínez Rodriguez Elche Alicante Spain 03203

Sponsors and Collaborators

  • University of Alicante

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prof. Dr. Alejandro Martínez-Rodríguez, Full Professor, University of Alicante
ClinicalTrials.gov Identifier:
NCT05567211
Other Study ID Numbers:
  • UA-2021-03-11
First Posted:
Oct 5, 2022
Last Update Posted:
Oct 7, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 7, 2022