Ignite Creation Date:
2024-05-06 @ 4:01 AM
Last Modification Date:
2024-10-26 @ 11:42 AM
Study NCT ID:
NCT02430467
Status:
COMPLETED
Last Update Posted:
2023-08-25
First Post:
2015-04-24
Brief Title:
Caregiver-Guided Pain Management Training in Palliative Care
Sponsor:
Duke University
Organization:
Duke University
Study Overview
Official Title:
Caregiver-Guided Pain Management Training in Palliative Care
Status:
COMPLETED
Status Verified Date:
2023-08
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 this study is to develop more effective ways to help patients and their caregivers cope with cancer pain The investigators are looking at the usefulness of a Caregiver-Guided Pain Management Training Intervention versus Pain Education
Detailed Description:
The primary aim of this study is to test the efficacy for the Caregiver-Guided Pain Management Training intervention to improve the caregivers self-efficacy for helping the patient manage pain Secondary aims include testing the effectiveness of the CG-PMT intervention to improve patient pain severity patient self-efficacy for pain management and patient psychological distress as well as short-term caregiver adjustment and caregiver adjustment following the patients death
In this multi-site study 236 dyads patients with cancer pain and their family caregivers will be randomized to either a Caregiver-Guided Pain Management Training protocol or to an Enhanced Treatment-as-Usual control condition Dyads in the Caregiver-Guided Pain Management condition will receive three one-hour sessions conducted via videoconference Dyads in the Enhanced Treatment-as-Usual condition will receive educational material about cancer pain and its management but will not receive any study-related treatment sessions Assessments will be conducted with patients and caregivers before and after treatment and with caregivers 3 months and 6 months following the patients death The primary hypothesis to be tested is that caregivers who receive the intervention will report significantly higher levels of self-efficacy for helping the patient manage pain than caregivers in the control condition Secondary aims will focus on a improvements in short-term caregiver adjustment as well as caregiver adjustment following the patients death and b patient pain severity self-efficacy for pain management and psychological distress
In this multi-site study 236 dyads patients with cancer pain and their family caregivers will be randomized to either a Caregiver-Guided Pain Management Training protocol or to an Enhanced Treatment-as-Usual control condition Dyads in the Caregiver-Guided Pain Management condition will receive three one-hour sessions conducted via videoconference Dyads in the Enhanced Treatment-as-Usual condition will receive educational material about cancer pain and its management but will not receive any study-related treatment sessions Assessments will be conducted with patients and caregivers before and after treatment and with caregivers 3 months and 6 months following the patients death The primary hypothesis to be tested is that caregivers who receive the intervention will report significantly higher levels of self-efficacy for helping the patient manage pain than caregivers in the control condition Secondary aims will focus on a improvements in short-term caregiver adjustment as well as caregiver adjustment following the patients death and b patient pain severity self-efficacy for pain management and psychological distress
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 |
|---|---|---|---|
| 1R01NR015348-01 | NIH | None | httpsreporternihgovquickSearch1R01NR015348-01 |