Addressing Cancer-Related Distress Through Survivorship Care

This study is looking at whether a special visit with a Physician Assistant (PA) at the start of cancer treatment can help reduce distress and improve quality of life for adults with cancer. This visit, called a Structured Survivorship Visit, uses your distress screening results to guide discussions about your emotional, physical, and practical needs. You might be able to join if you are 18 or older, have any type of cancer, are starting active treatment (like chemotherapy), and have a distress score of 4 or higher on a screening tool. The study aims to see if this visit helps with psychological distress and quality of life. Currently, the study is recruiting about 15 participants.

Study design
This is a single-arm study, meaning all participants receive the same intervention. It plans to enroll about 15 participants.
What's involved
You will complete questionnaires about your distress and quality of life. You will also have one Structured Survivorship Visit with a Physician Assistant.
Compensation
Not stated in the trial record.
Follow-up
Your psychological distress will be measured at the start, two weeks after the visit, and one month after the visit.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07673731

Addressing Cancer-Related Distress Through Survivorship Care in Community Oncology

Enrolling by Invitation
NAAges 18+InterventionalSupportive care
Ellis Medicine
~15 participants
Updated 2026-06-29 on ClinicalTrials.gov
What's tested:Structured Survivorship Visit

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in Psychological Distress as Measured by the NCCN Distress Thermometer and Problem List
Measured over Baseline, 2 weeks after survivorship visit, and 1 month after survivorship visit
Psychosocial Distress
Cancer
1 sites across 1 states
New York1

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Age 18 years and older.
Patients with histologically confirmed malignancy, any stage or type.
Beginning active therapy (either in oral or IV) for cancer at Ellis Medicine/Roswell Park Medical Oncology.
A score of ≥4 on the NCCN Distress Thermometer at screening.
Able and willing to provide written informed consent.
Ability to read and understand English sufficiently to complete study questionnaires.

Exclusion

Under the age of 18 years.
Patient is unable to provide informed consent.
Currently receiving ongoing therapy or have had treatment for cancer in the past (i.e., not a new start)
Significant cognitive impairment that would preclude completion of study questionnaires
  • Change in Psychological Distress as Measured by the NCCN Distress Thermometer and Problem ListBaseline, 2 weeks after survivorship visit, and 1 month after survivorship visit

    Psychological distress will be measured using the National Comprehensive Cancer Network (NCCN) Distress Thermometer and Problem List, a validated self-report measure in which participants rate their overall distress on a scale from 0 (no distress) to 10 (extreme distress). Change in distress scores from baseline to follow-up assessments will be evaluated.