Clinical trial Recruiting at 1 site Observational Ages 50 and up Women only

Bone health, muscle strength, and frailty in postmenopausal women of African descent with sickle cell trait

Official title: Bone Loss, Physical Function and Frailty in Older Women With Sickle Cell Trait

Run by UConn Health · NCT07083531 · Data updated 2026-11-12

We will see if postmenopausal women of African descent who have sickle cell trait are more likely to have thinner bones, weaker muscles, or greater frailty than women without the trait.

More Sickle Cell Disease trials

Quick facts

Study typeObservational
Ages50 Years and up
SexWomen only
Enrollment50 (estimated)
SponsorUConn Health
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Farmington, Connecticut)
StatusRecruiting
StartedAugust 23, 2022
Main results expectedAugust 23, 2025
Study endsAugust 23, 2025
Registry record updatedJuly 24, 2025
Trial IDNCT07083531 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are women of African descent aged 50 or older who are postmenopausal, not taking medications that alter bone metabolism, and without diagnosed sickle cell disease.

Probably not a fit

Men, younger or premenopausal women, people of other ancestries, those with documented sickle cell disease, or those taking bone-active medications are unlikely to be eligible or benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a cross-sectional comparison of about 50 postmenopausal women of African descent, grouping participants by hemoglobin genotype (normal versus sickle cell trait). Participants are age 50 or older and have not had a menstrual period for at least 12 months; SCT status will be determined as part of the visit if unknown. The study measures bone mineral density, skeletal muscle function, and clinical markers of frailty and compares these outcomes between groups. Individuals taking medications or with medical conditions that strongly affect bone metabolism or with documented sickle cell disease are excluded.

Why it matters

Potential benefit: If successful, the work could identify sickle cell trait as an overlooked risk factor that would support earlier screening or prevention to reduce fractures and frailty in affected women.

How similar studies have gone: This specific focus on sickle cell trait and bone/muscle outcomes is relatively novel, and prior evidence linking SCT to bone loss and frailty is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female of African Decent.
* Age 50 years or older.
* Lack of menstrual period for at least 12 consecutive months

Exclusion Criteria:

* Taking medications known to influence bone metabolism (e.g., glucocorticoids, hormonal therapy, cancer or chemotherapy meds, anti-resorptive medications or anabolic therapies).
* Known metabolic bone disorder (e.g., uncontrolled thyroid disease, hyperparathyroidism, Vitamin D deficiency)
* Taking an investigational drug
* Documented sickle cell disease

Where it's running

  • UConn Health
    Farmington, Connecticut, United States
    Recruiting

Study contacts

  • Principal investigator: Biree Andemariam, MD — UConn Health
  • Study coordinator: Zoe Green, BS
  • Email: zgreen@uchc.edu
  • Phone: 860.679.4656

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Collecting blood samples to study sickle cell disease

    This study is collecting blood samples from healthy people and those with sickle cell disease to see if new drugs can help stop red blood cells from sickling.

    Recruiting National Institutes of Health Clinical Center (CC) · Bethesda, Maryland · NCT00542230

  • Cerebrovascular Reactivity Testing with HD-DOT in Sickle Cell Patients

    This study tests whether high-density diffuse optical tomography can measure brain blood flow and oxygen use in people with sickle cell disease, to see how these signals relate to stroke risk.

    Recruiting Washington University School of Medicine · St Louis, Missouri · NCT07776444

  • Adapting and testing PEN-Plus in Zambian primary care

    Aiming to see if the PEN-Plus package can be adapted and used in two Zambian hospitals to better manage chronic diseases like heart disease, diabetes, hypertension, and sickle cell in primary care.

    Recruiting Centre for Infectious Disease Research in Zambia · Lusaka, Lusaka Province · NCT07753681

  • Newborn Sickle Cell Screening in Mozambique

    We’re testing a three-part plan to help babies in Mozambique get diagnosed early for sickle cell disease and start care quickly.

    Recruiting St. Jude Children's Research Hospital · Nhamatanda, Sofala · NCT07719972

  • Optimizing Hydroxyurea in Children with Sickle Cell in Africa

    This study tests whether raising hydroxyurea to a maximum tolerated dose is safe and beneficial for Ugandan children with sickle cell anemia already taking a fixed daily dose.

    Recruiting Phase 1/2 Children's Hospital Medical Center, Cincinnati · Kampala · NCT07708714

  • Hematopoietic stem cell editing to treat sickle cell disease

    This study tests whether a patient’s own blood stem cells can be edited to remove the sickle cell triggering gene and then returned to the patient.

    Recruiting Phase 1 Boston Children's Hospital · Boston, Massachusetts · NCT07708350

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.