Viewing Study NCT03210727



Ignite Creation Date: 2024-05-06 @ 10:18 AM
Last Modification Date: 2024-10-26 @ 12:27 PM
Study NCT ID: NCT03210727
Status: COMPLETED
Last Update Posted: 2018-09-20
First Post: 2017-07-03

Brief Title: CAREgiver Study for Patients Undergoing HSCT
Sponsor: Dartmouth-Hitchcock Medical Center
Organization: Dartmouth-Hitchcock Medical Center

Study Overview

Official Title: A Mixed Methods Descriptive Study Exploring the Needs and Preferences of Caregivers of Patients Undergoing Hematopoietic Stem Cell Transplantation HSCT
Status: COMPLETED
Status Verified Date: 2018-09
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 investigators will use a single arm design and deliver a new supportive intervention entitled Ready to Connect Actively Relax and Exercise CARE The purpose of the study is to describe the feasibility acceptability and potential effectiveness of the Ready to CARE intervention Effectiveness outcomes include caregiver self-efficacy distress and coping style and patient quality of life symptom burden and healthcare utilization
Detailed Description: During the first phase of this study the investigators enrolled caregivers of patients undergoing hematopoietic stem cell transplantation HSCT into a descriptive study The investigators used quantitative and qualitative measures to describe the caregivers self-efficacy distress and coping style and solicit their opinions about how to improve our supportive care for caregivers

Informed by those data the investigators now will study the effectiveness of the supportive intervention

The long-term goal of this research is to develop a pragmatic replicable intervention that supports caregivers and promotes the health and well-being of the caregiver-HSCT patient dyad

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