Ignite Creation Date:
2024-05-06 @ 8:28 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06396598
Status:
RECRUITING
Last Update Posted:
2024-05-02
First Post:
2024-04-12
Brief Title:
Electronic Symptom Monitoring Program for Triggered Palliative Referrals in Patients With Thoracic Cancer
Sponsor:
Ohio State University Comprehensive Cancer Center
Organization:
Ohio State University Comprehensive Cancer Center
Study Overview
Official Title:
SyMPLER Patient- and Caregiver-Triggered Palliative Referrals Via an Electronic Symptom Monitoring Program
Status:
RECRUITING
Status Verified Date:
2024-04
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:
This clinical trial evaluates earlier symptom management through remote electronic symptom monitoring such as through an app on patients phone and accessibility of palliative care self-referral by patients with thoracic cancer and caregivers by proxy legal representative Thoracic cancer occurs in the chest and often causes symptoms for patients Patients andor their caregivers are often unable to attend in-person clinic visits for various reasons The most frequently reported symptom by patients at initial palliative care consultations is pain and caregivers most common concerns are pain management for the patient stress reduction and fears about patient decline Earlier palliative care referral can help control these symptoms before they worsen providing a better quality of life for patients and caregivers improve physical and emotional functioning for patients and caregivers in cancer care This study may help researchers learn how an electronic symptom monitoring program may provide an earlier and more accessible way for patients with thoracic cancer to receive palliative care
Detailed Description:
PRIMARY OBJECTIVE
I Develop and assess feasibility of a remote electronic symptom monitoring program with a prompted option for palliative care self-referral for patients or caregivers by proxy after diagnosis of a thoracic malignancy
SECONDARY OBJECTIVE
I Evaluate palliative care referral patterns after implementation of a remote electronic symptom monitoring program
OUTLINE
Patients and their caregivers use the electronic symptom monitoring program to log symptoms once a week QW for 24 weeks Patients and their caregivers also watch a video and review education materials prior to starting the remote symptom monitoring program
After completion of study intervention participants are followed up to 2 years
I Develop and assess feasibility of a remote electronic symptom monitoring program with a prompted option for palliative care self-referral for patients or caregivers by proxy after diagnosis of a thoracic malignancy
SECONDARY OBJECTIVE
I Evaluate palliative care referral patterns after implementation of a remote electronic symptom monitoring program
OUTLINE
Patients and their caregivers use the electronic symptom monitoring program to log symptoms once a week QW for 24 weeks Patients and their caregivers also watch a video and review education materials prior to starting the remote symptom monitoring program
After completion of study intervention participants are followed up to 2 years
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| NCI-2024-00269 | REGISTRY | CTRP Clinical Trial Reporting Program | None |