Ignite Creation Date:
2025-12-24 @ 10:00 PM
Ignite Modification Date:
2026-01-02 @ 2:37 PM
Study NCT ID:
NCT02334332
Status:
WITHDRAWN
Last Update Posted:
2015-09-25
First Post:
2015-01-06
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Educational Brochure in Preparing Patients With Gastric Cancer and Their Caregivers for Recovery After Surgery
Sponsor:
City of Hope Medical Center
Organization:
Study Overview
Official Title:
Pilot Study of an Educational Brochure to Prepare Patients and Informal Caregivers for Recovery Following Gastrectomy
Status:
WITHDRAWN
Status Verified Date:
2015-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
No accrual
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This pilot clinical trial studies an educational brochure in preparing patients with gastric cancer and their caregivers for recovery after surgery. Giving an educational brochure may help prepare patients and their caregivers by improving knowledge about symptoms after surgery. It may also improve quality of life and reduce worry after surgery.
Detailed Description:
PRIMARY OBJECTIVES:
I. To pilot test an educational intervention in the form of a teaching brochure to prepare patients and informal caregivers for recovery following partial or total gastrectomy.
SECONDARY OBJECTIVES:
I. To describe preliminary effect of the intervention on patient-reported outcomes (PROs), informal caregiver-reported outcomes, and clinical/system outcomes.
OUTLINE: Participants are enrolled sequentially to 1 of 2 cohorts.
COHORT I: Participants receive standard post-operative care.
COHORT II: Participants receive a 2-page educational brochure after surgery and prior to discharge home.
After completion of study, participants are followed up for approximately 2 months.
I. To pilot test an educational intervention in the form of a teaching brochure to prepare patients and informal caregivers for recovery following partial or total gastrectomy.
SECONDARY OBJECTIVES:
I. To describe preliminary effect of the intervention on patient-reported outcomes (PROs), informal caregiver-reported outcomes, and clinical/system outcomes.
OUTLINE: Participants are enrolled sequentially to 1 of 2 cohorts.
COHORT I: Participants receive standard post-operative care.
COHORT II: Participants receive a 2-page educational brochure after surgery and prior to discharge home.
After completion of study, participants are followed up for approximately 2 months.
Study Oversight
Has Oversight DMC:
True
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?: