Home-Based Symptom Monitoring: Its Impact on Cancer Care Team Behaviors and Patient Outcomes

NCT00300001 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2006-08-25

No results posted yet for this study

Summary

The primary research objective of this protocol is to evaluate the impact of integrating a home-based symptom monitoring system in the day-to-day care of cancer patients in community settings on the frequency of supportive symptom interventions, symptom severity, and quality of life.

Conditions

Sponsors & Collaborators

  • Amgen

    collaborator INDUSTRY
  • Community Cancer Care

    lead OTHER

Principal Investigators

  • Dale E. Theobald, PhD, MD · Community Cancer Care, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31

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 NCT00300001 on ClinicalTrials.gov