ClinConnect ClinConnect Logo
Search / Trial NCT06305741

A Study of an Anxiety Intervention for Latino/Latina/Hispanic Older Adults With Cancer and Their Caregivers

Launched by MEMORIAL SLOAN KETTERING CANCER CENTER · Mar 5, 2024

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Anxiety Intervention Latino Caregivers 24 060

ClinConnect Summary

This clinical trial is looking at a special program designed to help reduce anxiety in older Latino adults who have cancer, as well as their caregivers. The goal is to see if this anxiety treatment is practical and effective for those who might be struggling with anxiety during their cancer journey. To participate, older adults need to be at least 65 years old, currently receiving cancer treatment or have finished treatment within the last 18 months, and identify as Latino or Hispanic. They also need to have a caregiver who is 40 or older and willing to take part in the study.

If you or someone you know might be eligible, participants can expect to join a supportive program that aims to help manage anxiety. It’s important to note that participants must be fluent in English or Spanish and willing to share their experiences. However, individuals currently undergoing psychotherapy or certain medications, or those severely impaired, may not be eligible. This study is actively recruiting participants, and your involvement could help improve support for older adults facing cancer and their caregivers.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Older Adults with Cancer (OAC)
  • As per medical record or self-report, is currently age 65 years or older
  • As per medical record or self-report, currently receiving active cancer treatment OR is within eighteen months of completing active treatment which includes surgery, chemotherapy, radiation, and immunotherapy.
  • As per self-report, identifies as Latino and/or Hispanic Ethnicity
  • Per self-report, has a primary informal caregiver (as defined by an unpaid individual who provides the patient with emotional, physical, and/or practical support) age 40 or older who is willing and able to participate in the study ; if a patient does not have a primary informal caregiver or if the caregiver does not or cannot participate, but meets all other inclusion criteria they will be allowed to enroll in the study
  • Scores ≥6 on the anxiety subscale of the Hospital Anxiety and Depression Scale (HADS)
  • * Per self-report, fluent in English and/or Spanish\*\* \*\* Language verification: Prior to enrollment, patients will be asked the following two questions by a Clinical Research Coordinator (CRC) to verify language fluency necessary for participation in the study:
  • 1. How well do you speak English and/or Spanish? (must respond "very well" or "well" when given the choices of Very well, Well, Not well, Not at all, Don't know, or Refused)
  • 2. What is your preferred language for healthcare? (must respond English and/or Spanish)
  • Caregiver
  • Per OAC report, is primary informal caregiver (as defined by an unpaid individual who provides the patient with emotional, physical, and/or practical support) for the eligible OAC patient
  • As per self-report, is age 40 years or older
  • * Per self-report, fluent in English and/or Spanish\*\* \*\* Language verification: Prior to enrollment, patients will be asked the following two questions by a Clinical Research Coordinator (CRC) to verify language fluency necessary for participation in the study:
  • 1. How well do you speak English and/or Spanish? (must respond "very well" or "well" when given the choices of Very well, Well, Not well, Not at all, Don't know, or Refused)
  • 2. What is your preferred language for healthcare? (must respond English and/or Spanish)
  • Exclusion Criteria:
  • OAC
  • As per medical record or self-report, currently receiving psychotherapy
  • As per medical record or self-report, taking psychotropic medications for \< 8 weeks prior to MAC Session 1 and/or anticipates changing their medication during the study
  • As per medical record or self-report, currently being treated for schizophrenia, substance use or dependence, and/or bi-polar disorder
  • Severely cognitively impaired as demonstrated by Blessed Orientation Memory Concentration score ≥ 9
  • Per research staff judgment and/or self-report, too ill or weak to complete study procedures
  • Per medical record or self-report, receiving hospice care at the time of enrollment
  • Caregiver
  • As per self-report, currently receiving psychotherapy
  • As per self-report, taking psychotropic medications for \< 8 weeks prior to MAC Session 1 and/or anticipates changing their medication during the study
  • As per self-report, currently being treated for schizophrenia, substance use or dependence, and/or bi-polar disorder
  • Severely cognitively impaired as demonstrated by Blessed Orientation Memory Concentration score ≥ 11
  • Per research staff judgment and/or self-report, too ill or weak to complete study procedures

About Memorial Sloan Kettering Cancer Center

Memorial Sloan Kettering Cancer Center (MSKCC) is a world-renowned institution dedicated to cancer treatment, research, and education. As a leading clinical trial sponsor, MSKCC focuses on advancing innovative cancer therapies through rigorous scientific investigation and collaboration. The center's multidisciplinary team of experts employs cutting-edge methodologies to design and conduct trials that aim to improve patient outcomes and enhance understanding of cancer biology. With a commitment to translating research findings into clinical practice, MSKCC plays a pivotal role in shaping the future of oncology care and ensuring that patients have access to the latest therapeutic advancements.

Locations

New York, New York, United States

Harrison, New York, United States

Middletown, New Jersey, United States

Montvale, New Jersey, United States

Rockville Centre, New York, United States

Basking Ridge, New Jersey, United States

Commack, New York, United States

Patients applied

0 patients applied

Trial Officials

Kelly McConnell, PhD

Principal Investigator

Memorial Sloan Kettering Cancer Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported