Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06543537
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-05
Brief Title:
Pilot Randomized Controlled Trial of a Collaborative Agenda-setting Intervention CASI for Patients With Ovarian Cancer
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Pilot Randomized Controlled Trial of a Collaborative Agenda-setting Intervention CASI for Patients With Ovarian Cancer
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This research is being done to test a new communication tool for people with ovarian cancer caregivers and clinicians
The name of the intervention in this research study is
-Collaborative Agenda-Setting Intervention CASI
The name of the intervention in this research study is
-Collaborative Agenda-Setting Intervention CASI
Detailed Description:
This two-arm parallel group-randomized research study is to test a new communication tool CASI for people with ovarian cancer caregivers and clinicians This is a pilot feasibility study which means this is the first time researchers are studying CASI Clinicians will be randomized into one of the two study groups Arm 1 or Arm 2 and patients and caregivers will be enrolled in the study arm to which their clinician has been randomized
The research study procedures include screening for eligibility audio recorded clinic visits and questionnaires
Participation in this research study is expected to last for up to 12 weeks for patients and caregivers and for up to 52 weeks for clinicians
It is expected that up to 112 people will take part in this research study including up to 50 patients 50 caregivers and 12 clinicians six dyads
The National Institute for Nursing Research is supporting this research by providing funding
The research study procedures include screening for eligibility audio recorded clinic visits and questionnaires
Participation in this research study is expected to last for up to 12 weeks for patients and caregivers and for up to 52 weeks for clinicians
It is expected that up to 112 people will take part in this research study including up to 50 patients 50 caregivers and 12 clinicians six dyads
The National Institute for Nursing Research is supporting this research by providing funding
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