N
← Back to Search
Sponsored

Accelerate Your Clinical Trial Recruitment

Reach thousands of high-intent patients matching your specific inclusion criteria.

Start Campaign
RECRUITING Not applicable ClinicalTrials.gov

A Study of a One-Time Counseling Session to Help Reduce Depression, Anxiety, and Distress in People With Cancer

Sponsor: Memorial Sloan Kettering Cancer Center • ClinicalTrials.gov ID: NCT07218250

Registry updated: 2026-09-30
Ad

Recruiting for Similar Conditions?

Sponsors are looking for patients like you. See if you qualify for compensated research studies.

Check Eligibility →

Description

The purpose of this study is to see if a Single Counseling Session for Cancer can help reduce psychosocial distress and improve quality of life in people with cancer who are waiting to receive ongoing counseling services (outpatient psychotherapy services). The Single Counseling Session for Cancer-which I will refer to as the "study counseling" during this call-is a one-session, 60-minute counseling program designed to reduce anxiety and depression symptoms in people with cancer who are waiting to receive outpatient psychotherapy services. The researchers will look at whether the study counseling is effective in participants and practical (feasible) for them to complete.

Interventions

  • Single Counseling Session (Behavioral)
    The one-time counseling session will be a problem-solving focused program that will try to strengthen the belief in the ability to manage the challenges of the cancer diagnosis and treatment
  • American Cancer Society booklet (Other)
    called "After Diagnosis: A Guide for Patients and Families" for review. Again, this booklet includes information about cancer, living with cancer, making treatment decisions, talking to others about cancer, cancer treatment, and questions for the cancer care team. It will be given in person or by email.

Eligibility criteria

Inclusion Criteria: * Patient must have pathologically confirmed cancer (per EMR). * Patient with localized or advanced cancer (per EMR). * Patient is on a waitlist of at least 2 weeks or more for MSK Counseling Center intake and will not complete a New Visit with a clinical psychologist prior to intervention (these patients will be replaced) (per EMR, patient's care team, or self-report) * Has not had and is not scheduled to have an appointment with an MSK psychiatrist or MSK Counseling Center advanced practice provider (per EMR, patient's care team, or self-report) * Age ≥ 18 (per EMR) * English fluency - Per self-report: How well do you speak English? * Agrees to be audio-recorded (per self-report) NOTE: Participants who report Very well are considered fluent. * Lives in New York, New Jersey, Connecticut, or Florida (per self-report). * Has no significant psychiatric disturbance sufficient to preclude completion of the assessment measures, interview, or informed consent (i.e., acute psychiatric symptoms which require urgent or extended individual treatment) (per EMR, patient's care team, or study team). * Has no presence of cognitive impairment disorder (i.e., delirium, dementia, or traumatic brain injury) sufficient to preclude meaningful informed consent and/or data collection (per EMR, patient's care team, study team, or per self-report of BOMC cognitive test). * Has no current active or passive suicidal ideation ((per EMR, patient's care team, study team, per item 9 of the PHQ-9, or the CSSRS).

Conditions

Breast Cancer

Locations

  • Memorial Sloan Kettering Basking Ridge (Consent Only) — Basking Ridge, New Jersey, United States
  • Memorial Sloan Kettering Monmouth (Consent Only) — Middletown, New Jersey, United States
  • Memorial Sloan Kettering Bergen (Consent Only) — Montvale, New Jersey, United States
  • Memorial Sloan Kettering Suffolk- Commack (Consent Only) — Commack, New York, United States
  • Memorial Sloan Kettering Westchester (Consent Only) — Harrison, New York, United States
  • Memorial Sloan Kettering Cancer Center (All Protocol Activities) — New York, New York, United States
  • Memorial Sloan Kettering Nassau (Consent Only) — Uniondale, New York, United States
Sponsored

Partner with Nurenyx

Showcase your study to thousands of motivated patients matching your criteria.

Learn More

Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record