Ignite Creation Date:
2024-05-06 @ 4:05 PM
Last Modification Date:
2024-10-26 @ 2:03 PM
Study NCT ID:
NCT04863157
Status:
COMPLETED
Last Update Posted:
2023-01-18
First Post:
2021-04-21
Brief Title:
Survivor-Sleep Health Information Program
Sponsor:
Dana-Farber Cancer Institute
Organization:
Dana-Farber Cancer Institute
Study Overview
Official Title:
A Sleep Intervention for Children After Cancer Survivor Sleep Health Information Program Survivor-SHIP
Status:
COMPLETED
Status Verified Date:
2023-01
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:
The purpose of the study is to learn if an educational program delivered to parentsguardians can help improve the sleep of children experiencing sleep problems after completing cancer treatment The name of the intervention is Survivor-SHIP Sleep Health Information Program
Detailed Description:
This study will evaluate Survivor-SHIP in a single-arm trial of 20 off-treatment childhood cancer survivors ages 5-12 The intervention is an adapted version of the family-centered Sleep Health Program designed at Seattle Childrens Hospital The program offers parents information about how to utilize evidence-based strategies for their childs sleep and has demonstrated success in a community-based sample of children with behavioral sleep problems Sessions will focus on providing parents with education about healthy sleep and setting targets for modifiable behaviors that can improve their childs sleep health
The study will include 3 education sessions taking place over videoconference Families will be asked to track their childs sleep using sleep diaries during the course of the program Prior to and following the program families will be asked to complete study questionnaires
The study will include 3 education sessions taking place over videoconference Families will be asked to track their childs sleep using sleep diaries during the course of the program Prior to and following the program families will be asked to complete study questionnaires
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None