Self-Management Survivorship Care in Stage I-III Non-small Cell Lung Cancer or Colorectal Cancer

  • STATUS
    Recruiting
  • participants needed
    414
  • sponsor
    City of Hope Medical Center
Updated on 19 February 2024
cancer
lung cancer
cancer treatment
carcinoma
cancer therapy
cancer care
colorectal cancer
non-small cell lung cancer
small cell lung cancer
stage iiic colorectal cancer ajcc v8
stage iib lung cancer ajcc v8
stage ib lung cancer ajcc v8
stage ia2 lung cancer ajcc v8
stage iiib lung cancer ajcc v8
stage iii lung cancer ajcc v8
stage ia3 lung cancer ajcc v8
stage i lung cancer ajcc v8
stage iiic lung cancer ajcc v8
stage iia colorectal cancer ajcc v8
stage ii colorectal cancer ajcc v8
stage iiib colorectal cancer ajcc v8
stage iii colorectal cancer ajcc v8
stage iiia lung cancer ajcc v8
stage iia lung cancer ajcc v8
stage ii lung cancer ajcc v8
stage i colorectal cancer ajcc v8
stage ia1 lung cancer ajcc v8

Summary

This phase III trial studies how well a telehealth self-management program works in improving survivorship care and outcomes in stage I-III non-small cell lung cancer or colorectal cancer survivors. Survivor self-management program focuses on coaching patients on follow-up care after cancer treatments. Participating in the program may improve knowledge and confidence about follow-up care, communication with cancer care and primary care doctors, and quality of life after cancer treatment in non-small cell lung cancer or colorectal cancer survivors.

Description

PRIMARY OBJECTIVES:

I. Determine the efficacy of the intervention on care coordination, communication, and primary care provider (PCP) knowledge, comparing the intervention and attention control arms at 4 and 8 months post-accrual.

II. Determine the efficacy of the intervention on survivor outcomes, comparing the intervention and attention control arms at 4 and 8 months post-accrual.

EXPLORATORY OBJECTIVE:

I. Assess the reach, efficacy, adoption, implementation, and maintenance (RE-AIM) of the intervention.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM I (SURVIVOR SELF-MANAGEMENT): Patients receive a personalized care plan/resource manual. Patients also participate in 5 telehealth sessions with a nurse over 60 minutes each for 4 months (months 1-4) about self-management skills building, then 3 maintenance telehealth sessions with a nurse over 60 minutes each for 3 months (months 5-7) for additional self-management skills building support. A copy of patient's care plan is also sent to their PCP.

ARM II (ATTENTION CONTROL): Patients receive an American Society of Clinical Oncology (ASCO) care plan. Patients also participate in 5 telehealth sessions with a nurse over 60 minutes each for 4 months (months 1-4) to review a handbook about life after cancer treatment, then 3 monthly telehealth sessions with a nurse over 60 minutes each for 3 months (months 5-7) to answer questions about the handbook. A copy of the ASCO care plan is also sent to their PCP.

After study initiation, patients are followed up at 4 and 8 months.

Details
Condition Stage III Lung Cancer AJCC v8, Stage IIIA Lung Cancer AJCC v8, Stage IIIB Lung Cancer AJCC v8, Stage IIIC Lung Cancer AJCC v8, Stage I Lung Cancer AJCC v8, Stage IA1 Lung Cancer AJCC v8, Stage IA2 Lung Cancer AJCC v8, Stage IA3 Lung Cancer AJCC v8, Stage IB Lung Cancer AJCC v8, Stage IIA Lung Cancer AJCC v8, Stage II Lung Cancer AJCC v8, Stage IIB Lung Cancer AJCC v8, Stage I Colorectal Cancer AJCC v8, Stage II Colorectal Cancer AJCC v8, Stage IIA Colorectal Cancer AJCC v8, Stage IIB Colorectal Cancer AJCC v8, Stage IIC Colorectal Cancer AJCC v8, Stage III Colorectal Cancer AJCC v8, Stage IIIA Colorectal Cancer AJCC v8, Stage IIIB Colorectal Cancer AJCC v8, Stage IIIC Colorectal Cancer AJCC v8, Lung Non-Small Cell Carcinoma
Age 18-100 years
Treatment Questionnaire Administration, Quality-of-Life Assessment, Survivorship Care Plan, Telemedicine
Clinical Study IdentifierNCT04428905
SponsorCity of Hope Medical Center
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Non-small cell lung cancer (NSCLC) and colorectal cancer survivors who are 4 months post-treatment completion
History of stage I-III disease
Ability to read or understand English
All subjects must have the ability to understand and the willingness to sign a written informed consent

Exclusion Criteria

Subjects, who in the opinion of the principal investigator (PI), may not be able to comply with the requirements of the study
Clear my responses

How to participate?

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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