Bone health, muscle strength, and frailty in postmenopausal women of African descent with sickle cell trait
Bone Loss, Physical Function and Frailty in Older Women With Sickle Cell Trait
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.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 50 Years and up |
| Sex | Female |
| Sponsor | UConn Health Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Farmington, Connecticut) |
| Trial ID | NCT07083531 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
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.
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 performed: 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.
Eligibility criteria
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 this trial is running
Farmington, Connecticut
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.