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Not yet recruiting NCT07711340

Diurnal Strength Variation

No phase Interventional Healthy Adult Exercise

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Time-driven dosing.
Who it may be relevant to
Registry conditions: Healthy Adult, Exercise. Basic parameters: 18 years — 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Exercise Timing and Lower Limb Biomechanics

Overview

Healthy individuals will be tested at different times of day to determine whether exercise at a non-expected time results in poorer performance.

Interventions

  • Behavioral Time-driven dosing
    Three hours earlier or later than usual exercise

Primary outcome measures

  • Isometric quadriceps strength [Time frame: 15 minutes]
Secondary outcome measures (2)
  • Isometric hamstring strength [Time frame: 15 minutes]
  • Isokinetic hamstring/quad strength [Time frame: 15 minutes]

Eligibility criteria

Inclusion criteria

  • Healthy
  • 18-25 years old
  • Lower body exercise three or more times per week, all at the same time of day (within 2 hour window)
  • Regular meal times (±1 hour window)
  • Regular sleep times (±1 hour window)

Exclusion criteria

  • Active or uncontrolled mental or physical health issues
  • Current musculoskeletal injury

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Single blind
Primary purpose
Basic science

Study locations

United States · 1 center
  • Stanford University — Stanford

Identifiers

NCT: NCT07711340 · 87320

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗