ClinicalTrials.gg
CompletedNCT07870434Updated Oct 13, 2026

The Metabolic Response of Unweighted Treadmill Walking

An interventional study of AlterG Treadmill and Metabolic Assessment in Metabolic Testing, sponsored by NYU Langone Health. Completed at 2 sites in United States. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by NYU Langone Health · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Jan 2026, registered Oct 2026).
Updated Oct 13, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This study will use an experimental quantitative research design. Participants will serve as their own control with a metabolic assessment by open circuit spirometry when walking on the Alter G treadmill for less than ten minutes per trial at 3 mph while supporting their entire body mass. Randomly assigned trials at 25%, 50%, 75% and 100% of body mass will be conducted under steady state conditions. All trials will be conducted in one session.

02

Conditions studied

  • Metabolic Testing
03

In context

Lead sponsor

NYU Langone Health is the lead sponsor of 1,421 studies on the registry; 254 are open to participants now.

Of its 231 completed or terminated interventional studies of FDA-regulated products, 195 (84%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • Apparently healthy college-age individuals
  • Able to walk at a moderate pace (3 mph)
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (actual)

Study arms

  • Experimental
    Metabolic Assessment during AlterG Treadmill Use

    Each participant will undergo a metabolic assessment by open circuit spirometry (to be performed by the Adelphi study team) when walking on an AlterG Treadmill for less than ten minutes per trial at 3 mph while supporting their entire body mass. The randomly assigned trials will be completed at 25%, 50%, 75%, and 100% of body mass under steady-state conditions.

    Other: AlterG Treadmill · Other: Metabolic Assessment

Interventions

  • OtherAlterG Treadmill

    Participants will walk on an AlterG Treadmill for less than ten minutes per trial at 3 mph while supporting their entire body mass. The randomly assigned trials will be completed at 25%, 50%, 75%, and 100% of body mass under steady-state conditions.

  • OtherMetabolic Assessment

    Conducted using a Parvo Medics TrueOne 2400 metabolic cart and standard heart rate monitor, one way valve mouthpiece, and nose clip.

06

What researchers measure

Primary outcomes

  1. Oxygen Consumption at 25% Body Weight

    Time frame: Day 1

  2. Oxygen Consumption at 50% Body Weight

    Time frame: Day 1

  3. Oxygen Consumption at 75% Body Weight

    Time frame: Day 1

  4. Oxygen Consumption at 100% Body Weight

    Time frame: Day 1

  5. Heart Rate at 25% Body Weight

    Time frame: Day 1

  6. Heart Rate at 50% Body Weight

    Time frame: Day 1

  7. Heart Rate at 75% Body Weight

    Time frame: Day 1

  8. Heart Rate at 100% Body Weight

    Time frame: Day 1

  9. Ventilation at 25% Body Weight

    Time frame: Day 1

  10. Ventilation at 50% Body Weight

    Time frame: Day 1

  11. Ventilation at 75% Body Weight

    Time frame: Day 1

  12. Ventilation at 100% Body Weight

    Time frame: Day 1

  13. Carbon Dioxide Production at 25% Body Weight

    Time frame: Day 1

  14. Carbon Dioxide Production at 50% Body Weight

    Time frame: Day 1

  15. Carbon Dioxide Production at 75% Body Weight

    Time frame: Day 1

  16. Carbon Dioxide Production at 100% Body Weight

    Time frame: Day 1

07

Study locations

2 sites
  • NYU Langone Health
    East Meadow, New York 11554, United States
  • Adelphi University
    Garden City, New York 11530, United States
08

References and documents

Individual participant data

Plan to share: Yes — The de-identified participant data from the final research dataset will be shared upon reasonable request beginning 9 to 36 months after publication or as required by a condition of awards or supporting agreements, provided the requesting investigator executes a data use agreement with NYU Langone Health. This instance of data sharing will also require separate IRB review as well as review from NYU Langone's Data Sharing Strategy Board (DSSB). Requests should be directed to: mark.grossman@nyulangone.org. The protocol and statistical analysis plan will be posted on Clinicaltrials.gov only as required by federal regulation or supporting awards and agreements.

Supporting information: Study protocol, Statistical analysis plan

Time frame: Beginning 9 months and ending 36 months following article publication or as required by a condition of awards and agreements supporting the research.

Access criteria: Requests should be directed to mark.grossman@nyulangone.org. To gain access, data requestors will need to sign a data access agreement. This instance of data sharing will also require separate IRB review as well as review from NYU Langone's DSSB.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07870434
Lead sponsor
NYU Langone Health
Collaborators
Adelphi University
Responsible party
Sponsor
First posted
Oct 13, 2026
Start date
Jan 6, 2026
Primary completion
Jan 13, 2026
Completion
Jan 13, 2026
Last update
Oct 13, 2026

Study contacts

Bob Otto
principal investigator · Adelphi University
Mark Grossman, MD
principal investigator · NYU Langone Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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