A Study Of Sleep Enhancement Strategies In Post -Surgical Patients Using The Actigraph Device

Overview

About this study

The purpose of this study is to determine if  existing sleep enhancement strategies are effective in improving sleep quality or quantity compared to individuals who do not receive those interventions on the same post surgical inpatient unit, using Actigraph® wearable activity tracker.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Individuals who have undergone surgery at MCF and are admitted as inpatients on 4S.

  • Between ages 18 and 80 years.

  • Agreeable to wear the device.

Exclusion Criteria: 

  • Unable to provide consent independently.

  • There are no identifiable exclusion criteria for wearing the sleep tracker. This device will not interfere with other devices used to monitor or assess patients during their hospital stay.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 6/19/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Jacksonville, Fla.

Mayo Clinic principal investigator

Brittany Burke, P.T., D.P.T., GCS

Contact us for the latest status

More information

Publications

Publications are currently not available

Additional contact information

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