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Effectiveness of an Individualized Symptom Education Program (ISEP)

NCT00275353 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 144

Last updated 2006-05-26

No results posted yet for this study

Summary

The purpose of this study is to examine whether an Individualized Symptom Education Program (ISEP) is helpful to women to manage their symptoms when they are receiving radiation therapy for gynecological cancer.

It is expected that women who participate in the ISEP program will be better able to manage their symptoms and exprience less distress than women who receive usual care.

Conditions

Interventions

BEHAVIORAL

Individualized Symptom Education

Sponsors & Collaborators

  • Canadian Cancer Trials Group

    collaborator NETWORK

  • University of Toronto

    lead OTHER

Principal Investigators

  • Karima Velji, RN, MSc, AOCN, PhD(C) · University of Toronto

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-07-31
Completion
2006-02-28

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT00275353 on ClinicalTrials.gov