Peds SM-THINk: Nursing Interventions to Improve Discharge Outcomes

NCT03539978 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 486

Last updated 2019-12-12

No results posted yet for this study

Summary

This study focuses on the delivery of discharge education by clinical nurses to improve parent and family self-management in the home environment. This study tests an discharge method (SM-THINk protocol) designed to improve the quality of care for hospitalized pediatric patients at the time of discharge, enhance the child's and family's experience, and decrease length of stay and health care utilization (ED visit or re-admission). The SM-THINk protocol is an enhancement to the standard clinical practice and will be implemented for all subjects on two Children's Hospital of Wisconsin (CHW) nursing units. This enhancement will require additional training of the nurses prior to implementation of the research project. This research determines the effectiveness of the training enhanced discharge method. The training is independent from the research project and will evaluate effectiveness of this training. For the enhanced discharge method, clinical nurses on the study units will be trained to deliver the Self-Management Transition to Home (SM-THINk protocol), which is based on the family self-management discharge preparation previously developed and tested by the study team.

Conditions

  • Pediatric ALL

Interventions

OTHER

SM-THINk

Patients will receive the SM-THINk enhanced discharge method.

Sponsors & Collaborators

  • Clinical & Translational Science Institute

    collaborator UNKNOWN
  • Marquette University

    collaborator OTHER
  • Children's Hospital and Health System Foundation, Wisconsin

    collaborator OTHER
  • University of Wisconsin, Milwaukee

    collaborator OTHER
  • Medical College of Wisconsin

    lead OTHER

Principal Investigators

  • Stacee Lerret, PhD · Medical College of Wisconsin

Eligibility

Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-30
Primary Completion
2019-02-20
Completion
2019-04-20

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03539978 on ClinicalTrials.gov