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ACTIVE NOT RECRUITING NA

Circadian Health Regulation and Optimization for Rejuvenation Outcomes

NCT07203196 · View on ClinicalTrials.gov ↗

Study Summary

In this single arm intervention trial, the investigators will assess the impact of a personalized lifestyle plan, centered on supporting biological rhythms, on blood sugar levels, physical, cognitive and immune function in older adults with a habitual eating window of 12 hours or more, and elevated blood glucose levels. All participants will be provided with a personalized circadian rhythm optimization plan (CRO) centered on improving (1) diet, (2) exercise (3) sleep habits based on their body's natural rhythms. The study includes a 2-week screening/baseline assessments, with follow-up health assessments at 2-months.

Interventions

  • BEHAVIORAL Circadian Rhythm Optimization

Study Locations (1)

California

  • University of California San Diego — La Jolla

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2025-10-22
Est. Completion 2026-04-01
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07203196

The ClinicalTrials.gov registry entry for NCT07203196 describes a study currently listed as active not recruiting. 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 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Salk Institute for Biological Studies, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Time Restricted Eating appearing as the primary indexed condition, and to 1 intervention — of which Circadian Rhythm Optimization 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: NCT07203196 reports 1 study location spanning 1 distinct geographic area — top geographies include California. 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 NCT07203196 about?

NCT07203196 is a clinical study titled "Circadian Health Regulation and Optimization for Rejuvenation Outcomes". In this single arm intervention trial, the investigators will assess the impact of a personalized lifestyle plan, centered on supporting biological rhythms, on blood sugar levels, physical, cognitive and immune function in older adults with a habitual eating window of 12 hours or more, and elevated ...

What is the current status of trial NCT07203196?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 16 participants. The study started on 2025-10-22. Estimated completion is 2026-04-01.

What conditions does trial NCT07203196 study?

This clinical trial studies the following conditions: Time Restricted Eating, Circadian Dysregulation, Blood Sugar; High, Aging, Healthy, Blood Sugar (Glucose) Control. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07203196?

The interventions under investigation include: Circadian Rhythm Optimization (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07203196?

This trial is sponsored by Salk Institute for Biological Studies, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07203196 being conducted?

This trial has 1 study location across California. 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