Sleep Improvement Intervention for Hospitalized Antepartum Patients

Sam Houston State University

Status: Completed

Conditions: Sleep Disturbance in Hospitalized Antepartum Patients

Treatments: Behavioral: Sleep Improvement Protocol Intervention for Hospitalized Antepartum Patients

Study type: Interventional

Funder types: Other

Identifiers

NCT04485728

IRB-2020-83

Details and patient eligibility

About

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).

Enrollment: 40 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

40 participants in 2 patient groups

Sleep Improvement Intervention

Experimental group

Treatment:

Behavioral: Sleep Improvement Protocol Intervention for Hospitalized Antepartum Patients

Standard of Care (Control)

No Intervention group