SymptomCare@Home: Deconstructing an Effective Symptom Management Intervention

NCT02779725 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 884

Last updated 2023-11-08

No results posted yet for this study

Summary

This project will determine the most important and cost effective components of SymptomCare@Home, a new approach to cancer chemotherapy symptom care that has been shown to reduce problematic symptoms through automated daily monitoring, self-management coaching, and oncology team follow-up care using decisional support for patients at home when their symptoms are most likely at their worse. Once the key parts of the intervention and its cost effectiveness are known, it can be moved into everyday cancer care.

Conditions

Interventions

BEHAVIORAL

SCC

Automated self-management coaching paired to symptom reports during daily symptom monitoring call

BEHAVIORAL

Nurse Practitioner

Alerts generate if a patient reports symptoms above pre-set thresholds during daily symptom reporting calls . These alerts are monitored and follow up is given by a Nurse Practitioner.

BEHAVIORAL

DSS

A Clinical Decision Support System (DSS), based on evidenced based guidelines, will be used to assist the nurse practitioner in follow up to symptom alerts.

BEHAVIORAL

AT

An activity tracker will be provided to evaluate its use, acceptability and impact on fatigue severity. The purpose of providing the activity tracker is to extend the self-management coaching intervention given when participants report fatigue and receive coaching about exercise as part of the intervention.

BEHAVIORAL

Symptom Severity

Automated patient-reporting of 11 common cancer treatment symptoms

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Huntsman Cancer Institute

    collaborator OTHER
  • Emory University

    collaborator OTHER
  • University of Utah

    lead OTHER

Principal Investigators

  • Kathleen Mooney, PhD · University of Utah

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-07
Primary Completion
2020-03-31
Completion
2022-09-30

Countries

  • United States

Study Locations

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Entities

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 NCT02779725 on ClinicalTrials.gov