Sleep Improvement Intervention for Hospitalized Antepartum Patients
Not Applicable
Completed
- Conditions
- Sleep Disturbance in Hospitalized Antepartum Patients
- Registration Number
- NCT04485728
- Lead Sponsor
- Sam Houston State University
- Brief Summary
This project seeks to further study the effects of a hospital-based protocol for improving sleep in high-risk antepartum patients as piloted by Lee and Gay (2017).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
- speak, read, and write English
- medically stable
- 20 weeks' gestation or greater
- viable fetus
- hospitalized at least 24 hours
Exclusion Criteria
- Do not speak, read, and write English
- Medically unstable
- Less than 20 weeks' gestation
- Nonviable fetus
- Hospitalized less than 24 hours
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Level of satisfaction with the intervention as assessed by a Likert assessment Day 7 The scale ranges from 0-5 with 5 being extremely satisfied
Number of patients who use the sleep improvement intervention Day 7
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Memorial Hermann Texas Medical Center
🇺🇸Houston, Texas, United States
Memorial Hermann Texas Medical Center🇺🇸Houston, Texas, United States