Viewing Study NCT00002563



Ignite Creation Date: 2024-05-05 @ 11:08 AM
Last Modification Date: 2024-10-26 @ 9:03 AM
Study NCT ID: NCT00002563
Status: COMPLETED
Last Update Posted: 2013-04-10
First Post: 1999-11-01

Brief Title: SWOG-9208 Quality of Life and Health Status in Patients With Stage I or Stage II Hodgkins Disease
Sponsor: SWOG Cancer Research Network
Organization: SWOG Cancer Research Network

Study Overview

Official Title: Health Status and Quality of Life in Patients With Early Stage Hodgkins Disease A Companion Study to SWOG-9133
Status: COMPLETED
Status Verified Date: 2013-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: RATIONALE Quality-of-life assessment in patients undergoing cancer treatment may help determine the intermediate- and long-term effects of treatment on patients with cancer

PURPOSE This clinical trial studies the impact of therapy on the health status and quality of life of patients with stage I or stage II Hodgkins disease who are receiving radiation therapy with or without chemotherapy
Detailed Description: OBJECTIVES I Evaluate prospectively the health status and quality of life of patients with Stage IIIA Hodgkins disease randomized on protocol SWOG-9133 CLB-9391 to treatment with subtotal nodal irradiation with vs without 3 courses of doxorubicinvinblastine II Describe the short-term effects of these treatments on these patients and compare their impact on quality of life ie patient symptom status health status fatigue III Evaluate the intermediate and long-term effects of these treatments on these patients and compare their impact on quality-of-life outcomes over 5 years

OUTLINE Quality-of-Life Assessment Cancer Rehabilitation Evaluation System Short Form CARES-SF Symptom and Personal Information Questionnaire including Symptom Distress Scale MOS SF-36 Fatigue Scale MOS SF-36 Health Perception Rating Demographics Cover Sheet

PROJECTED ACCRUAL Approximately 500 patients will be accrued over 7 years

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
CLB-9497 OTHER CALGB httpsreporternihgovquickSearchU10CA032102
U10CA032102 NIH None None
SWOG-9208 OTHER None None