Improving Sleep In Midlife Women

🩺 Protocol Summary

This study purpose of this study to see how consuming pistachios and completing a health intervention session a study therapist may improve sleep health in midlife women with poor sleep. Participants in this study will be asked to consume a study snack for about one month, complete a health education session with a study therapist and record information about their sleep. At baseline and after the intervention we will collect information about sleep, alertness, body composition, and blood lipids.

Primary Research Facility: University of Texas Medical Branch (Galveston, Texas)

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Poor Sleep Quality?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged between 45 Years and 65 Years? • (Protocol specifies female participants only)

🔍 Protocol Specified Age Range: 45 Years to 65 Years

Able to attend required clinic visits at University of Texas Medical Branch (Galveston, Texas)?

🔍 Logistical Requirement: Site at University of Texas Medical Branch

📍 Primary Site Map

Site: University of Texas Medical Branch — Galveston, Texas

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.