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ACTIVE NOT RECRUITING
NCT06610968
NA

Acute Vitamin D Supplementation on Testosterone in Females

Sponsor: University of Southern California

View on ClinicalTrials.gov

Summary

Participation will take place over two visits to the Clinical Exercise Research Center (CERC) at the University of Southern California Health Sciences Campus. On the first visit, height, weight, and body composition by bioelectrical impedance are recorded. Questionnaires and withdrawal of a sample of blood (1 tablespoon) are also completed. The intervention begins the day following the first visit. The intervention protocol consists of three weeks of consuming either a placebo capsule or a 5000 IU Vitamin D capsule daily and completing a daily survey. The second visit to CERC immediately follows the 3-weeks intervention. In this visit, the same blood sampling protocol will be completed. The assignment of the intervention will be randomized (i.e., rolling a die), and participants are blinded to group assignment.

Official title: Effects of Acute Vitamin D Supplementation on Testosterone in Young, Healthy Females: A Pilot Study

Key Details

Gender

FEMALE

Age Range

18 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2025-07-01

Completion Date

2026-09-30

Last Updated

2026-03-25

Healthy Volunteers

Yes

Interventions

DIETARY_SUPPLEMENT

Vitamin D (Cholecalciferol )

5000 IU Vitamin D (as cholecalciferol) capsules (Vitamin D3 125 mcg \[5,000 IU\], Pure Encapsulation, LLC) daily

DIETARY_SUPPLEMENT

Placebo Group

One placebo capsule (Zeebo Imagine, Zeebo) daily.

Locations (1)

University of Southern California Health Sciences Campus Center for Health Professions

Los Angeles, California, United States