Starting a Testosterone and Exercise Program After Hip Injury
This study is a randomized controlled double-blinded multi-center clinical trial enrolling female hip fracture patients who are 65 and older. It will compare the effects of six months of supervised exercise training combined with daily topical testosterone gel, to six months of supervised exercise and inactive gel, and to Enhanced Usual Care. One third of the participants will receive topical testosterone gel and a supervised exercise training program; one third will receive topical inactive gel and a supervised exercise training program; one third will receive a home exercise program. All participants will receive nutritional counseling, and calcium and vitamin D supplements.
- Hip Fracture
- Eligible Ages
- Over 65 Years
- Eligible Genders
- Accepts Healthy Volunteers
- Female 65 years and older.
- Surgical repair of a non-pathologic fracture of the proximal femur (Including: intracapsular, intertrochanteric, and subtrochanteric fractures) with a surgical repair date that is within 6-14 weeks at screening, and within 16 weeks at randomization.
- Community-dwelling or in assisted living prior to the hip fracture event.
- Functional impairment at the time of screening, defined as a modified Physical Performance Score (mPPT) of 12-28.
- Serum total testosterone level <40 ng/dL.
- Cognitive impairment or dementia of severity sufficient to interfere with ability to fully participate in the study or provide one's own informed consent, or a score of 11 or greater on the Short Blessed Test of Orientation, Memory and Concentration.
- Residence too far from research center (specific distance to be determined by each site) or planned travel greater than 2 weeks within the next 9 months.
- Anticipated to be permanently living in a nursing home at the time of randomization.
- Use of progestin or androgen containing compound within the previous 6 months.
- Treatment with systemic corticosteroids (daily dose > 5 mg prednisone or equivalent) for at least 90 days within the previous 12 months.
- Visual or hearing impairments that interfere with following directions for research procedures.
- Active or unstable cardiopulmonary disease (recent MI, unstable angina, class III or IV CHF) within prior 6 months, which would limit full participation in the study.
- Respiratory disease requiring chronic continuous oxygen therapy, or oxygen therapy during walking or exercise, which would limit full participation in this study.
- History of thrombotic event requiring treatment.
- Musculoskeletal or neurological conditions that limit participation in this study, could be made worse by exercise training, or not expected to improve with exercise.
- Lower extremity amputation other than toes.
- Severe lower extremity pain or ulceration that could limit full participation in this study.
- History of a hormone dependent neoplasia.
- History of HIV or active viral hepatitis.
- End Stage Renal Disease on dialysis or GFR<15 ml/min.
- Allergy to gel components.
- Recent history of alcohol or substance abuse, or current alcohol intake of ≥ 10 drinks/week.
- Planned joint surgery during the intervention period.
- Participation in another research study that in the site investigator's judgement could interfere or conflict with STEP-HI research assessments or interventions.
- Current use of aldactone, flutamide or leflunomide.
- GDS score ≥ 12 at the screening assessment.
- Uncontrolled hypertention, defined as a systolic BP > 160 mmHg or diastolic BP > 95 mmHg, on at least two occasions.
- Elevated liver transaminase levels ≥ 2.5 times above normal range.
- Erythrocytosis with hematocrit > 51% (all sites except UCD) or ≥ 52% at UCD.
- Severe anemia defined as Hgb < 7gm/dL.
- Uncontrolled diabetes defined as HgbA1C > 10%.
- Untreated or unstable thyroid disease, with serum TSH level ≥ 10 mIU/L or TSH level ≤ 0.4 mIU/L.
- Site investigator's judgement that the participant would not be able to complete research procedures or interventions.
- Phase 3
- Study Type
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Masking Description
- Participants, investigators, and study staff conducting the interventions will be aware of the exercise group assignment. A Blinded Outcomes Assessor will be masked to study group assignment. Only the study pharmacist, an unblinded study physician, and Data Coordinating Center staff will be unblinded to gel treatment assignment.
Exercise + Testosterone (EX + T)
|Supervised exercise training 2 times per week and topical testosterone 1% gel (12.5 mg per pump depression) daily, both for six months duration.||
Exercise + Placebo (EX + P)
|Supervised exercise training 2 times per week and placebo gel daily, both for six months duration.||
Enhanced Usual Care (EUC)
|Home exercise program 3 times per week and monthly health education modules, both for six months duration.||
- NCT ID
- Washington University School of Medicine
Study ContactEllen F Binder, MD
Hip fractures are common among older women and can have a devastating impact on their ability to remain independent. A clinically important functional decline and failure to recover following a hip fracture has been documented as late as a year after the fracture, even among women who were functioning at high levels before the event. Age-associated androgen deficiency in women contributes to deficits in muscle mass, strength and power that are common in this patient population before the fracture, and are exacerbated afterward. A pilot study of testosterone (T) supplementation in elderly female hip fracture patients has demonstrated the feasibility of T treatment in this population, and showed gains in lean body mass (LBM) and muscle strength with active drug, compared to placebo. The benefits of exercise in restoring muscle strength and physical function after a hip fracture have been documented. However, it remains unclear whether T treatment can augment the effects of exercise on mobility and patient-reported function after hip fracture.
The STEP-HI study is a 3-group, multi-center, randomized, placebo-controlled, double-blinded, parallel group clinical trial in older female hip fracture patients. 300 female hip fracture patients, age 65 years and older, will be enrolled from 6 clinical sites, using objective screening criteria for T deficiency (serum total testosterone level < 40 ng/dL) and physical frailty (Modified Physical Performance Test (PPT) Score of 12-28). The trial will compare the effects of Enhanced Usual Care with home exercises and no gel treatment (EUC), supervised exercise training (EX) with inactive (placebo) gel (EX+P), and EX combined with T therapy (EX+T), to ascertain the incremental impact of adding T to EX in older adult women with a recent hip fracture. The study team will carefully monitor testosterone levels, adverse events, biochemical parameters, and factors related to adherence to the interventions.
Information from this study has the potential to alter treatment of hip fracture in older women, a problem that contributes to significant morbidity and mortality, and has a large public health impact. The STEP-HI study is highly aligned with NIA's mission of identifying interventions that target common geriatric conditions and improve treatment options for older adults with multiple morbidities or risk factors.