Sleep Improvement Intervention for Hospitalized Antepartum Patients

Not Applicable

Completed

• Conditions: Sleep Disturbance in Hospitalized Antepartum Patients
• Interventions: Behavioral: Sleep Improvement Protocol Intervention for 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

Study Timeline

• Study First Submitted: 2020-07-21
• Study First Submitted QC: 2020-07-21
• Study First Posted: 2020-07-24
• Study Start: 2022-03-11
• Primary Completion: 2022-07-31
• Study Completion: 2023-01-31
• Status Verified: 2023-07
• Last Update Submitted: 2023-07-31
• Last Update Posted: 2023-08-02

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

Arm && Interventions

Group	Intervention	Description
Sleep Improvement Intervention	Sleep Improvement Protocol Intervention for Hospitalized Antepartum Patients	-

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

Trial Locations

Locations (1)

Memorial Hermann Texas Medical Center; 🇺🇸 Houston, Texas, United States