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Supportive Care for Lung Cancer
N/A
Waitlist Available
Led By Manali I Patel, MD
Research Sponsored by Palo Alto Veterans Institute for Research
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9 months after patient enrollment
Awards & highlights
Study Summary
This trial will test a new way of proactively managing symptoms and delivering evidence-based care to patients with thoracic cancers. The goal is to improve patient satisfaction, quality of life, and use of healthcare resources.
Who is the study for?
This trial is for lung cancer patients at VA Palo Alto, both newly diagnosed and those already receiving care. It's not open to those who won't get their oncology care at this center or can't consent to participate.Check my eligibility
What is being tested?
The study tests whether weekly phone calls to check on symptoms can improve patient satisfaction, increase engagement in their own care, enhance quality of life, and affect healthcare resource use.See study design
What are the potential side effects?
Since the intervention involves telephone assessments rather than medications or procedures, there are no direct medical side effects; however, some may experience discomfort discussing symptoms.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 9 months after patient enrollment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 months after patient enrollment
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Symptom documentation
Secondary outcome measures
Change in Patient Activation using the validated Patient Activation Measure
Change in Quality of Life using the Functional Assessment of Cancer Therapy - Lung survey
Change in patient satisfaction with decision-making using the Satisfaction with Decision Survey
+3 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Weekly telephone symptom assessmentExperimental Treatment1 Intervention
Each patient who is enrolled in the intervention will receive a weekly phone call from the Research Assistant for a total of 9 months to assess symptoms using the Edmonton Symptom Assessment Scale. Results of the symptom assessments will be provided to the clinic staff (RN and MD) for review each week. Symptom assessments will be documented into an encrypted, HIPAA compliant digital platform which provides longitudinal symptom data management and also provides symptom assessment tools for the clinical team in their intervention strategies.
In addition, patients will complete symptom and quality of life surveys at 0, 3, 6 and 9 months.
Group II: Control ArmActive Control1 Intervention
Patients randomized to usual clinical care will receive standard of care for thoracic malignancies as provided by the VA Palo Alto Health Care System. Patients will complete outcome surveys at 0, 3, 6, and 9 months.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Weekly telephone symptom assessment
2017
N/A
~60
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Who is running the clinical trial?
Palo Alto Veterans Institute for ResearchLead Sponsor
52 Previous Clinical Trials
7,845 Total Patients Enrolled
Carevive Systems, Inc.Industry Sponsor
15 Previous Clinical Trials
994 Total Patients Enrolled
Manali I Patel, MDPrincipal InvestigatorFaculty
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Control Arm
- Group 2: Weekly telephone symptom assessment
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any vacancies in the current clinical trial?
"Clinicaltrials.gov suggests that this clinical trial is not currently enrolling patients, with the initial posting dating back to August 20th 2017 and last update occurring on October 25th 2022. Although current recruitment has concluded for this particular study, there are 649 other trials in progress at present."
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