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Improving Sleep in the Neurology In-Patient Population (I_SLEEP)

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University of Pennsylvania

Status

Completed

Conditions

Sleep

Treatments

Other: Sleep friendly order set
Other: Patient sleep menu

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

We aim to test multiple interventions to improve sleep for Neurology inpatients, including 1) a sleep-friendly order set, and 2) a sleep menu. We will collect patient sleep data, including duration and quality, via actigraphy devices (FitBits). We will also conduct qualitative patient surveys to understand the impact of these interventions.

Enrollment

145 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18
  • 24 hours after admission to the general neurology (ward) service at the Hospital of the University of Pennsylvania
  • Patients who are determined by the primary team to be clinically stable enough to forego serial overnight vital signs monitoring and neuro checks.
  • Clinical stability criteria:
  • Symptomatic stability >24h after admission (no new or progressive neurologic symptoms for >24 hours)
  • Vital signs stability on admission for > 24h while admitted
  • Ability to verbally consent to study participation

Exclusion criteria

  • Any medical or psychological conditions that, in the opinion of the investigator, would compromise the subject's safety or successful participation in the study.
  • Any additional clinical factors felt by the team to be incompatible with specific orders including requiring serial vital signs monitoring and neuro checks overnight

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

145 participants in 2 patient groups

Standard of care
No Intervention group
Sleep intervention
Experimental group
Treatment:
Other: Patient sleep menu
Other: Sleep friendly order set

Trial contacts and locations

1

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Central trial contact

Laura Stein, MD; Nichole Gallatti

Data sourced from clinicaltrials.gov

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