ExLOH: Physical Exercise as a Sustainability Tool in Men With Dysmetabolic Hypogonadism

Sponsor
Istituto Auxologico Italiano (Other)
Overall Status
Recruiting
CT.gov ID
NCT06094036
Collaborator
(none)
72
1
2
23.7
3

Study Details

Study Description

Brief Summary

Aim of this project is to delineate sustainable physical exercise programs and to assess the effects of such programs mainly on endocrine-metabolic and neurovegetative outcomes in a cohort of men with metabolic syndrome-related late-onset central hypogonadism.

Participants will undergo a personalised exercise program. After 6 months they will be subdivided into two groups, according to the weekly physical activity volume actually performed (above or below 600 MET·minutes/week). Changes in endocrine-metabolic and neurovegetative outcomes will be compared between the two groups.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Structured and personalized program of physical exercise
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
72 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Physical Exercise as a Sustainability Tool in Men Affected With Metabolic Syndrome-related Late-onset Central Hypogonadism: Role of Endocrine-metabolic and Neurovegetative Outcomes
Actual Study Start Date :
Jan 11, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: weekly physical activity volume performed above 600 MET·minutes/week

Exercise program requiring clear definition of modality, intensity, frequency, duration and progression of exercise, tailored on patient's clinical conditions and goals.

Behavioral: Structured and personalized program of physical exercise
In line with the most recent guidelines, exercise prescription will require the clear definition of modality, intensity, frequency, duration and progression of exercise, tailored on patient's clinical conditions and goals. This intervention will be accompanied by a nutrition program aiming for proper dietary habits in terms of both quantity and quality.

Other: weekly physical activity volume performed below 600 MET·minutes/week

Exercise program requiring clear definition of modality, intensity, frequency, duration and progression of exercise, tailored on patient's clinical conditions and goals.

Behavioral: Structured and personalized program of physical exercise
In line with the most recent guidelines, exercise prescription will require the clear definition of modality, intensity, frequency, duration and progression of exercise, tailored on patient's clinical conditions and goals. This intervention will be accompanied by a nutrition program aiming for proper dietary habits in terms of both quantity and quality.

Outcome Measures

Primary Outcome Measures

  1. change in hypothalamic-pituitary-gonadal axis function [6 months]

    particularly testosterone levels (nmol/l)

Secondary Outcome Measures

  1. Change in body composition [6 months]

    percentage of fat mass and free fat mass

  2. Change in serum skeletal isoenzyme of alkaline phosphatase [6 months]

    Change in serum skeletal isoenzyme of alkaline phosphatase concentration (ug/l)

  3. Change in C-terminal telopeptide of type I collagen [6 months]

    Change in C-terminal telopeptide of type I collagen concentration (ng/l)

  4. Change in erythrocyte sedimentation rate [6 months]

    Change in erythrocyte sedimentation rate (mm/h)

  5. Change in C-reactive protein [6 months]

    Change in C-reactive protein concentration (mg/l)

  6. Change in total cholesterol [6 months]

    Change in total cholesterol concentration (mg/dl)

  7. Change in HDL cholesterol [6 months]

    Change in HDL cholesterol concentration (mg/dl)

  8. Change in triglycerides [6 months]

    Change in triglycerides concentration (mg/dl)

  9. Change in glucose profile [6 months]

    glycemia (mg/dl)

  10. Change in kidney function [6 months]

    creatinine (mg/dl)

  11. Change in aspartate aminotransferase [6 months]

    Change in aspartate aminotransferase concentration (U/L)

  12. Change in alanine aminotransferase [6 months]

    Change in alanine aminotransferase concentration (U/L)

  13. Change in cardiac autonomic regulation [6 months]

    Autonomic Nervous System Index (ANSI)

  14. Change in nutrition quality [6 months]

    American Heart Association (AHA) Diet Score

  15. Change in perception of stress, fatigue, and somatic symptoms [6 months]

    short version of 4SQ questionnaire considering 4 specific symptoms (total score ranging from 0 to 40)

  16. Change in weekly physical activity volume [6 months]

    short version of International Physical Activity Questionnaire, which focuses on intensity (nominally estimated in Metabolic Equivalents - MET - according to the type of activity) and duration (in minutes) of physical activity. The following levels will be considered: brisk walking (≈ 3.3 METs), other modalities of activity of moderate intensity (≈ 4.0 METs), and activities of vigorous intensity (≈ 8.0 METs).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • diagnosis of late-onset central hypogonadism: total T levels < 8 nmol/L (or < 12 nmol/L in the presence of calculated free T < 225 pmol/L) combined with sexual symptoms (erectile dysfunction, low libido and loss of waking erections) [12];

  • diagnosis of metabolic syndrome, defined as association of waist circumference (WC) > 94 cm and at least two among the following criteria: triglycerides ≥ 150 mg/dl, HDL-C < 40 mg/dl, glucose > 100 mg/dl, blood pressure (BP) ≥ 130/85 mmHg [33];

  • ability to give informed consent, in accordance with good clinical practice rules and applicable national laws.

Exclusion Criteria:
  • History of hypothalamus-pituitary organic disorders and/or testicular diseases;

  • impossibility to assess cardiac autonomic regulation due to arrhythmias and/or current treatment for heart rate (HR) control (e.g., beta-blockers, antiarrhythmics);

  • impossibility to undergo clinical assessment;

  • impossibility or contraindications to perform exercise program (for instance, psychiatric disorders, severe musculoskeletal diseases, arrhythmias);

  • inability to give informed consent or unwillingness to be enrolled in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituto Auxologico Italiano IRCCS Milan Italy

Sponsors and Collaborators

  • Istituto Auxologico Italiano

Investigators

  • Principal Investigator: Daniela Lucini, MD, PhD, University of Milan; Istituto Auxologico Italiano, IRCCS

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Istituto Auxologico Italiano
ClinicalTrials.gov Identifier:
NCT06094036
Other Study ID Numbers:
  • 45C202
First Posted:
Oct 23, 2023
Last Update Posted:
Oct 23, 2023
Last Verified:
Oct 1, 2023
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 23, 2023