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N/A Completed N=16 Basic Science

Optimizing Ankle Exoskeleton Assistance for Walking Across the Life Span

Source: ClinicalTrials.gov NCT04033146 ↗
Enrolled (actual)
16
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcomePrimary: Net Metabolic Rate (Watts/kg) — 3.30; 3.47; 3.86; 4.18 watts/kg — p=<0.001

Summary

The investigators seek to determine whether ankle exoskeletons can reduce metabolic energy expenditure during walking for users across the age-spectrum.

Outcome Measures

OutcomeResultp-value
PRIMARY
Net Metabolic Rate (Watts/kg)
3.30; 3.47; 3.86; 4.18; 3.72; 4.34 <0.001 sig

Eligibility Criteria

Inclusion Criteria

  • Subjects must be able to walk for 60 minutes in a 90-minute time frame.
  • Subjects are apparently free of cardiovascular, metabolic, and renal disease, which includes no signs or symptoms suggestive of cardiovascular, metabolic or renal disease.
  • Subjects have no current musculoskeletal injury.
  • Subjects need to be either 18-45 or 65+ years old.

These criteria meet the American College of Sports Medicine's 2015 guidelines for participant health screening prior to joining a moderate or moderate-to-vigorous exercise protocol. (Riebe et al., 2015).

Exclusion Criteria

  • Have dementia or an inability to give informed consent
  • Have a musculoskeletal injury or feel pain while walking
  • Have a history of dizziness and/or balance problems
  • Have cardiovascular, heart, metabolic, or renal disease, or respiratory problems
  • Smoke cigarettes
  • Asthma
  • Feel pain or discomfort in the chest, neck, jaw, arms during rest or exercise
  • Have orthopnea or paroxysmal nocturnal dyspnea
  • Have ankle edema
  • Have palpitations or tachycardia
  • Have a heart murmur
  • Have had a heart attack
  • Have diabetes
  • Have a pace maker
  • Have unusual shortness of breath with usual activities
  • Are <18 or 46-64 years of age
  • Do not speak or understand English
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04033146). 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. Informational only — not medical advice.

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