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COMPLETED NA

Duration of Physical Inactivity and Postprandial Lipid Metabolism

NCT06407050 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to investigate the effect of different periods of physical inactivity on postprandial lipid metabolism in the morning after exercise by measuring plasma triglyceride levels and fat oxidation (burning). The study is a crossover intervention with all healthy participants performing three trials varying in length of physical inactive (4 hours, 8 hours, and 12 hours). All trials include a physical activity control phase (\>8,500 steps/24hr), a physical inactive phase, a moderate intensity cycling session, and a high-fat tolerance test.

Conditions Studied

Interventions

  • BEHAVIORAL 4 hours of physical inactivity
  • BEHAVIORAL 8 hours of physical inactivity
  • BEHAVIORAL 12 hours of physical inactivity

Study Locations (1)

Texas

  • The University of Texas at Austin — Austin

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2024-04-01
Est. Completion 2024-11-01
Phase NA

Sponsor

University of Texas at Austin

225 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06407050

The ClinicalTrials.gov registry entry for NCT06407050 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Texas at Austin, which has 225 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Metabolism appearing as the primary indexed condition, and to 3 interventions — of which 4 hours of physical inactivity is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06407050 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06407050 about?

NCT06407050 is a clinical study titled "Duration of Physical Inactivity and Postprandial Lipid Metabolism". The purpose of the study is to investigate the effect of different periods of physical inactivity on postprandial lipid metabolism in the morning after exercise by measuring plasma triglyceride levels and fat oxidation (burning). The study is a crossover intervention with all healthy participants pe...

What is the current status of trial NCT06407050?

This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2024-04-01. Estimated completion is 2024-11-01.

What conditions does trial NCT06407050 study?

This clinical trial studies the following conditions: Metabolism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06407050?

The interventions under investigation include: 4 hours of physical inactivity (BEHAVIORAL), 8 hours of physical inactivity (BEHAVIORAL), 12 hours of physical inactivity (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06407050?

This trial is sponsored by University of Texas at Austin, which has 225 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06407050 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial