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Comparison of Lifestyle Markers Between Women With and Without Polycystic Ovary Syndrome

NCT01859663 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to identify lifestyle factors associated with PCOS and understand how diet and activity levels impact features of PCOS. The secondary aim is to examine psychosocial factors (e.g., health beliefs) of women with PCOS.

Study Locations (3)

New York

  • Human Metabolic Research Unit, Cornell University — Ithaca
  • Strong Fertility Center — Rochester
  • CRC at University of Rochester Medical Center — Rochester

Trial Details

FieldValue
Enrollment Target 126 participants
Start Date 2013-05
Est. Completion 2022-05

Sponsor

Cornell University

50 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01859663

The ClinicalTrials.gov registry entry for NCT01859663 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 126 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cornell University, which has 50 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Physical Activity appearing as the primary indexed condition, and to 0 interventions. 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: NCT01859663 reports 3 study locations spanning 1 distinct geographic area — top geographies include New York. 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 NCT01859663 about?

NCT01859663 is a clinical study titled "Comparison of Lifestyle Markers Between Women With and Without Polycystic Ovary Syndrome". The purpose of the study is to identify lifestyle factors associated with PCOS and understand how diet and activity levels impact features of PCOS. The secondary aim is to examine psychosocial factors (e.g., health beliefs) of women with PCOS.

What is the current status of trial NCT01859663?

This trial is currently completed. The enrollment target is 126 participants. The study started on 2013-05. Estimated completion is 2022-05.

What conditions does trial NCT01859663 study?

This clinical trial studies the following conditions: Physical Activity, Polycystic Ovary Syndrome, Dietary Habits. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT01859663?

This trial is sponsored by Cornell University, which has 50 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01859663 being conducted?

This trial has 3 study locations across New York. 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