RecruitingNot ApplicableNCT06279013

Comparing Telephone Symptom Monitoring Interventions for Managing Symptoms and Psychological Distress During Oral Anti-Cancer Treatment

Managing Symptoms and Psychological Distress During Oral Anti-Cancer Treatment


Sponsor

NRG Oncology

Enrollment

600 participants

Start Date

Oct 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

In this clinical trial, symptom monitoring (interactive voice response \[IVR\] is compared to automated telephone symptom management \[ATSM\] and telephone interpersonal counseling \[TIPC\]) for reducing symptom burden and psychological distress (depressive and anxiety symptoms) among people receiving oral anti-cancer treatment. Symptoms are the number one driver of treatment interruptions and unscheduled health services use. To reduce the risk of these events, symptom monitoring and management are necessary. However, these services are not implemented routinely, especially in the community oncology settings. Further, depressive and anxiety symptoms are a key barrier to enacting symptom self-management strategies. IVR is a form of symptom monitoring where patients, when called, enter their symptom ratings over the phone. Their symptom summary is sent to their provider, and patients may be advised to reach out to their oncology provider, based on their symptoms. The ATSM intervention combines IVR assessments with a Symptom Management and Survivorship educational handbook with self-management strategies. Patients receiving ATSM enter their symptom ratings over the phone and have their symptoms reported to their provider, but patients are also directed to the handbook for strategies to manage elevated symptoms. Patients receiving ATSM who report being anxious, discouraged, or sad will also receive TIPC, which targets psychological distress and its connection to social support and interpersonal communication. Information gathered from this study may help researchers learn more about the best ways to manage patient symptoms and improve patient outcomes.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Counseling, a behavioral approach called Health Education, and others for people with hematopoietic and lymphatic system neoplasm and malignant solid neoplasm. The study is currently recruiting participants at 34 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERCounseling

Receive TIPC

BEHAVIORALHealth Education

Receive handbook

OTHERInterview

Ancillary studies

OTHERMedical Chart Review

Ancillary studies

OTHERMonitoring

Receive IVR symptom monitoring

OTHERQuestionnaire Administration

Ancillary studies


Locations(34)

Cancer Center at Saint Joseph's

Phoenix, Arizona, United States

CARTI Cancer Center

Little Rock, Arkansas, United States

Phoebe Putney Memorial Hospital

Albany, Georgia, United States

Augusta Oncology Associates PC-D'Antignac

Augusta, Georgia, United States

Augusta University Medical Center

Augusta, Georgia, United States

Queen's Cancer Cenrer - POB I

Honolulu, Hawaii, United States

Queen's Medical Center

Honolulu, Hawaii, United States

Queen's Cancer Center - Kuakini

Honolulu, Hawaii, United States

The Queen's Medical Center - West Oahu

‘Ewa Beach, Hawaii, United States

John H Stroger Jr Hospital of Cook County

Chicago, Illinois, United States

Carle at The Riverfront

Danville, Illinois, United States

Carle Physician Group-Effingham

Effingham, Illinois, United States

Carle Physician Group-Mattoon/Charleston

Mattoon, Illinois, United States

Carle Cancer Center

Urbana, Illinois, United States

Central Care Cancer Center - Garden City

Garden City, Kansas, United States

University Medical Center New Orleans

New Orleans, Louisiana, United States

Lake Regional Hospital

Osage Beach, Missouri, United States

University of New Mexico Cancer Center

Albuquerque, New Mexico, United States

AnMed Health Cancer Center

Anderson, South Carolina, United States

Medical University of South Carolina

Charleston, South Carolina, United States

Prisma Health Cancer Institute - Butternut

Greenville, South Carolina, United States

Prisma Health Cancer Institute - Faris

Greenville, South Carolina, United States

Prisma Health Greenville Memorial Hospital

Greenville, South Carolina, United States

Prisma Health Cancer Institute - Eastside

Greenville, South Carolina, United States

Langlade Hospital and Cancer Center

Antigo, Wisconsin, United States

Aspirus Medford Hospital

Medford, Wisconsin, United States

Aspirus Cancer Care - James Beck Cancer Center

Rhinelander, Wisconsin, United States

Aspirus Cancer Care - Stevens Point

Stevens Point, Wisconsin, United States

Aspirus Regional Cancer Center

Wausau, Wisconsin, United States

Aspirus Cancer Care - Wisconsin Rapids

Wisconsin Rapids, Wisconsin, United States

Puerto Rico Hematology Oncology Group

Bayamón, Puerto Rico

Doctors Cancer Center

Manati, Puerto Rico

Centro Comprensivo de Cancer de UPR

San Juan, Puerto Rico

PROncology

San Juan, Puerto Rico

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06279013


Related Trials