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Phase 2 N=84 Randomized Quadruple-blind Treatment

Multimodality Intervention for Function and Metabolism in SCI

Spinal Cord Injuries

Enrolled (actual)
84
Serious AEs
11.3%
Results posted
May 2026
Primary outcome: Primary: Change From Baseline in VO2 Peak (L/Min) Achieved During Arm Ergometry Exercise Alone — 0.11; 0.09 L/min

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Testosterone Undecanoate (Drug); hybrid exercise (Behavioral)
Age
Adult, Older Adult · 19+ yrs
Sex
All
Sponsor
Brigham and Women's Hospital
Primary completion
Jan 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in VO2 Peak (L/Min) Achieved During Arm Ergometry Exercise Alone
0.11; 0.09
PRIMARY
Change From Baseline in VO2 Peak (mL/kg/Min) Achieved During Arm Ergometry Exercise Alone
1.27; 0.88
SECONDARY
Change From Baseline in VO2 Peak (L/Min) Achieved During FES-LC Exercise Alone
0.06; 0.02
SECONDARY
Change From Baseline in VO2 Peak (mL/kg/Min) Achieved During FES-LC Exercise Alone
0.76; 0.48
SECONDARY
Change From Baseline in VO2 Peak (L/Min) Achieved During Combined FES-LC and AE Exercise
0.04; 0
SECONDARY
Change From Baseline in VO2 Peak (mL/kg/Min) Achieved During Combined FES-LC and AE Exercise
0.12; 1.89
SECONDARY
Change From Baseline in Work Rate Max During Arm Ergometry Alone
10.74; 6.49
SECONDARY
Change From Baseline in Work Rate Max During FES-LC Exercise Alone
1.98; 0.28
SECONDARY
Change From Baseline in Work Rate Max During Combined FES-LC + AE Exercise
8.91; 5.76
SECONDARY
Change From Baseline in the One Repetition Maximum (1-RM) Voluntary Strength in the Chest Press Exercise
45.1; 14.83
SECONDARY
Change From Baseline in the Muscle Endurance in the Chest Press Exercise
-0.26; -0.33
SECONDARY
Change From Baseline in the Whole Body Lean Mass Measured Using Dual Energy X-ray Absorptiometry (DXA)
2.21; 0.38
SECONDARY
Change From Baseline in the Upper Extremity Lean Tissue Mass Measured Using DXA
0.31; 0.01
SECONDARY
Change From Baseline in the Lower Extremity Lean Tissue Mass Measured Using DXA
1.28; 0.37
SECONDARY
Change From Baseline in the Trunk Lean Tissue Mass Measured Using DXA
0.60; 0.02
SECONDARY
Change From Baseline in the Appendicular Lean Tissue Mass Measured Using DXA
1.61; 0.37
SECONDARY
Change From Baseline in Fasting Glucose
4.52; -3.34
SECONDARY
Change From Baseline in Hemoglobin A1C
0.03; -0.02
SECONDARY
Change From Baseline Homeostatic Model Assessment for Insulin Resistance
0.52; -0.86
SECONDARY
Change From Baseline in Total Cholesterol
0.71; -2.02
SECONDARY
Change From Baseline in Low-density Lipoprotein
0.57; -1.89
SECONDARY
Change From Baseline in Non-HDL Cholesterol
1.80; -2.41
SECONDARY
Change From Baseline in HDL Cholesterol
-1.22; 0.48
SECONDARY
Change From Baseline in Triglycerides
7.77; -6.01
SECONDARY
Change From Baseline in Inflammatory Markers
-1157.18; 1602.67
SECONDARY
Change From Baseline in Self-reported Function and Mobility (SCI-FI) (Basic Mobility Standardized Score: 31.97 - 68.48), With a Higher Score Indicating Better Mobility
-0.12; 1.67
SECONDARY
Change From Baseline in Depressive Symptoms, Ascertained Using the Patient Health Questionnaire - 9 (PHQ-9) (Score: 0-27), With a Higher Score Indicating More Severe Depression
0.17; 0.80
SECONDARY
Change From Baseline in Pain and Its Impact on Life, Ascertained Using the Brief Pain Inventory (BPI) (Score:0 - 10), With a Higher Score Indicating More Pain
0.07; 0.35
SECONDARY
Change From Baseline in Loneliness, Using a 3-item Loneliness Questionnaire (Score: 3-9), With a Higher Score Indicating More Loneliness
0.18; 0.23
SECONDARY
Change From Baseline in Satisfaction With Life, Ascertained Using the Satisfaction With Life Scale (SWLS) (Score: 5 - 35), With a Higher Score Indicating More Satisfaction With Life
0.25; 0.50
SECONDARY
Change From Baseline in Anxiety Ascertained Using the Generalized Anxiety Disorder - 7 Scale (GAD-7) (Score: 0 - 21), With a Higher Score Indicating Worse Anxiety
0.80; 0.80

Summary

The proposed phase 2 trial a randomized, placebo-controlled, parallel group trial in persons with cervical or thoracic SCI, AIS grade A, B, C, or D, 6 months or later after injury. The trial will test the hypothesis that a Home-Based Multimodality Functional Recovery and Metabolic Health Enhancement Program that addresses multiple pathophysiologic factors in SCI and includes functional electrical stimulation during leg cycling (FES-LC) plus arm ergometry and an androgen will be more efficacious than functional electrical stimulation during leg cycling (FES-LC) plus arm ergometry plus placebo in improving aerobic capacity, function, metabolism, bone health, and wellbeing.

Eligibility Criteria

INCLUSION CRITERIA

  • Men and women, 19 to 70 years
  • Confirmed cervical and thoracic, AIS A-D who are at least 6 months post-injury and who use a wheelchair as their primary mobility mode
  • Medically stable, able to follow directions
  • Able to provide informed consent.
  • For females of reproductive potential who are sexually active: use of highly effective contraception for at least 1 month prior to Day 1 and agreement to use such a method during study participation and for an additional 12 weeks after the end of intervention.

EXCLUSION CRITERIA

  • Upper extremity musculoskeletal conditions (such as advanced rotator cuff pathology or carpal tunnel syndrome) or neurological disorder that in the assessment of the study investigator would prevent the participant from performing the prescribed arm ergometry.
  • Current fractures in the upper and lower extremity
  • In accordance with the Endocrine Society and ISSAM Guidelines25,52, we will exclude individuals with a contraindication for androgen use:
  • History of prostate or breast cancer
  • Prostate nodule or induration on digital rectal examination (DRE)
  • Prostate specific antigen (PSA) > 4 ng/ml or > 3 ng/ml in individuals at high risk of prostate cancer such as African Americans or those with family history of prostate cancer in first degree relatives, unless there has been a negative prostate biopsy within 3 months
  • Hematocrit > 48%
  • Conditions that would render exercise and FES unsafe or unfeasible such as severe autonomic dysreflexia, severe pressure sores, severe spasticity and severe pain.
  • Body mass index (BMI) > 45 kg/m2
  • Renal dysfunction as indicated by GFR of 3 x upper limit of normal
  • Poorly controlled diabetes as indicated by hemoglobin (Hb)-A1c greater than 9.0% or diabetes requiring insulin therapy
  • Blood thinners such as Coumadin, heparin, rivaroxaban (Xarelto), dabigatran (Pradaxa), lovenox (subcutaneous heparin), apixaban (Eliquis) (aspirin, plavix and other anti-platelet agents are allowed)
  • Systolic blood pressure (BP) > 170 or diastolic BP > 100 mm Hg
  • Current grade 2 or greater pressure ulcers at relevant contact sites
  • Pressure sores or open wounds on the areas that restricts their participation
  • Because the safety of testosterone has not been established in pregnancy and lactation, we will exclude pregnant or lactating women and women of childbearing potential who are sexually active but are unwilling or unable to use a reliable form of contraception. We will perform a blood test to exclude pregnancy at the time of enrollment.
  • Participation in a structured exercise program currently or in the past 2 months and unwilling to stop the structured exercise program if ongoing at time of screening. Specifically, participation in a structured exercise program, currently or in the past 2 months, that involves progressive resistance exercise training of moderate to high intensity or regular endurance exercise of moderate to high intensity, and unwillingness to stop the structured exercise program if ongoing at time of screening.
  • Inability or unwillingness to participate in the exercise training or the assessments of muscle performance and physical performance
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03576001). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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