Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 10:07 PM
Ignite Modification Date: 2025-12-24 @ 10:07 PM
NCT ID: NCT02204735
Eligibility Criteria: Inclusion Criteria: * body mass index (BMI) between 27 and 45 kg/m2 * normal self-reported daily (weekday and weekend) wake-up time between 5 am and 8 am * normal, self-reported weekend wake-up time within two hours of their normal, self-reported weekday wake-up time * regularly (at least five nights/week) get at least six total hours of self-reported sleep Exclusion Criteria: * report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q) * report being unable to walk for 2 blocks (1/4 mile) without stopping * are currently participating in a weight loss program and/or taking weight loss medication or lost \> 5% of body weight during the past 6 months * are diagnosed with type 1 or 2 diabetes * have had bariatric surgery or are planning to have bariatric surgery within the next 4 months * intend to move outside of the metropolitan area within the time frame of the investigation * are pregnant, lactating, \< 6 months post-partum, or plan to become pregnant during the investigation * are taking mediation to aid in sleep * are shift workers/alternative shift workers that work outside of 7 am and 7 pm * have a metal allergy (which would prevent the ability of participant to wear the SenseWear® armband from BodyMedia® used in the proposed study).
Healthy Volunteers: True
Sex: ALL
Minimum Age: 25 Years
Maximum Age: 65 Years
Study: NCT02204735
Study Brief:
Protocol Section: NCT02204735