Viewing Study NCT00056069



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00056069
Status: COMPLETED
Last Update Posted: 2015-05-07
First Post: 2003-03-06

Brief Title: Study of the Physical and Emotional Needs of Parents Caring for Children Receiving Chemotherapy for Acute Lymphoblastic Leukemia
Sponsor: Childrens Oncology Group
Organization: Childrens Oncology Group

Study Overview

Official Title: Differences in Parental Caregiving Demands in Childhood Acute Lymphoblastic Leukemia by Length of Infusion Therapy
Status: COMPLETED
Status Verified Date: 2015-05
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 Studying the physical and emotional needs of parents who are caring for children receiving chemotherapy for cancer may help doctors plan effective treatments for the patient that allow for improved quality of life of the patients family

PURPOSE This clinical trial is studying the different physical and emotional needs of parents whose children are undergoing chemotherapy for acute lymphoblastic leukemia either in an outpatient clinic or in the hospital
Detailed Description: OBJECTIVES

Compare the caregiving demands reported by parents of children with acute lymphoblastic leukemia receiving methotrexate on 2 different infusion schedules inpatient care vs outpatient care
Compare the change in caregiving demands on these parents over time in terms of physical and emotional care the need to make family arrangements the need to communicate about the childs care the need to gather information about the childs health status and the effect on family well-being

OUTLINE Participants complete questionnaires regarding caregiver demands and family information over 25-30 minutes within 3-4 months of the initiation of the childs treatment and at the completion of the first year of the childs treatment

PROJECTED ACCRUAL A total of 164 participants will be accrued for this study within 08 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
U10CA095861 NIH CTRP Clinical Trial Reporting Program httpsreporternihgovquickSearchU10CA095861
COG-ACCL01P3 OTHER None None
CDR0000271934 OTHER None None
NCI-2012-02522 REGISTRY None None