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OpenTrials
Completed

NCT Number: NCT04485728

Sleep Improvement Intervention for Hospitalized Antepartum Patients

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).

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Memorial Hermann Texas Medical Center

Houston, Texas, 77030, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Sleep Improvement Protocol Intervention for Hospitalized Antepartum Patients

Behavioral

Patients are getting sleep hygiene education and a sleep hygiene kit.

Primary outcomes

  1. Number of patients who use the sleep improvement intervention

    Time frame: Day 7

  2. Level of satisfaction with the intervention as assessed by a Likert assessment

    Time frame: Day 7

    The scale ranges from 0-5 with 5 being extremely satisfied

Sponsors and collaborators

Lead sponsor

Sam Houston State University

Other

Collaborators

  • Memorial Hermann Texas Medical Center
  • The University of Texas Health Science Center, Houston

Registry information

Important dates

Study start
2022
Primary completion
2022
Study completion
2023
First posted
Jul 24, 2020
Registry last updated
Aug 2, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.