Actively Recruiting

Phase 4
Age: 40Years - 55Years
FEMALE
Healthy Volunteers
NCT06745466

Disentangling the Effects of Daily Stress, Sleep, and Sex Hormones on Accelerated Vascular Aging in Midlife Women

Led by University of Delaware · Updated on 2026-05-01

30

Participants Needed

1

Research Sites

150 weeks

Total Duration

On this page

Sponsors

U

University of Delaware

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to identify the impact of estradiol (E2) on the associations between (a) responsivity to daily stress or (b) sleep variability with vascular function in midlife premenopausal women.

CONDITIONS

Official Title

Disentangling the Effects of Daily Stress, Sleep, and Sex Hormones on Accelerated Vascular Aging in Midlife Women

Who Can Participate

Age: 40Years - 55Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female
  • Age between 40 and 55 years
  • Premenopausal status
Not Eligible

You will not qualify if you...

  • Pregnant, planning to become pregnant, or breastfeeding
  • Peri- or post-menopausal status
  • Unstable or diagnosed chronic diseases including cardiovascular, metabolic, renal, hepatic, autonomic, autoimmune, or dermatological conditions
  • Current or lifetime major psychiatric illness such as major depressive disorder, bipolar disorder, schizophrenia, or eating disorders
  • History of hysterectomy, polycystic ovary syndrome, endometrial hyperplasia, irregular menstrual cycles, or endometrial ablation
  • Suspected obstructive sleep apnea (STOP-Bang score >3) or insomnia (Insomnia Severity Index score >15)
  • Current or recent (within 8 weeks) use of medications affecting cardiovascular function or sleep health
  • Changes in medication use including new or adjusted doses
  • Body mass index over 35 kg/m2
  • Use of tobacco or nicotine products including vaping and e-cigarettes
  • Night-time or rotating shift work within the last 3 months
  • Trans-meridian travel during enrollment and testing periods
  • Known allergies to study drugs
  • Current use of long-acting reversible contraception (e.g., IUDs, implants)
  • Known latex allergy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Delaware

Newark, Delaware, United States, 19713

Actively Recruiting

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Research Team

J

Jody Greaney, PhD

CONTACT

V

Virginia Nuckols, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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