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Recruiting NCT06608862

The Impact of Hormonal Contraceptive Use and Lifestyle Factors on Fracture Risk and Bone Quality in Young Female Adults

Observational Osteoporosis Osteopenia Fracture Reduction Body Composition

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Osteoporosis, Osteopenia, Fracture Reduction, Body Composition. Basic parameters: 18 years — 35 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Germany
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Impact of Hormonal Contraceptive Use, Body Composition, Muscular Strength and Iron Status on Fracture Risk and Bone Quality in Adult Females from 18-35 Years

Overview

The study on hand is based on a cross-sectional design and aims to acquire 1) descriptive data on the physical state and health condition of female soldiers in the German armed forces. 2) a possible influence of different contraceptive methods as well as physical activity, body composition, strength, nutrition, and hemoglobin levels on bone health should be investigated.

Primary outcome measures

  • T-Score [Time frame: Measured at baseline and at 12 months after enrollment]

Eligibility criteria

Inclusion criteria

  • 18 - 35 years
  • female
  • willing to participate under a pseudonym
  • occupational soldiers
  • free from chronic or acute musculoskeletal injury

Exclusion criteria

  • for the bioelectrical impedance: electronic implants like defibrillator, pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Ecologic or community

Study locations

Germany · 1 center
  • University of the Bundeswehr Munich — Munich

Identifiers

NCT: NCT06608862 · Female Health

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗