Geriatric Evaluation and Management With Survivorship Health Education for Older Survivors of Cancer, GEM-S Trial
University of Rochester · with National Cancer Institute (NCI) · NCT05006482
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 3
- Target enrollment
- 668
- US sites recruiting
- 44
- Study start
- March 21, 2023
- Record last updated
- January 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This phase III trial compares the effect of geriatric evaluation and management with survivorship health education (GEM-S) to usual care on patient-reported physical function in older survivors of cancer. Survivorship care for older adults of cancer usually consists of getting advice from their doctor. This advice may include how to do their daily activities, so they are less tired or how to manage multiple diseases, or long-term side effects from treatment. GEM-S may help improve the physical ability to perform activities of daily living, mental well-being, and memory in older survivors of cancer after chemotherapy. This study may help doctors learn if including GEM-S in their practices improves physical, mental and memory functions in their patients. The study may also help to understand how such care affects cancer patients and their caregivers' quality of life.
Being studied: Best Practice; Comprehensive Geriatric Assessment; Educational Intervention; Exercise Intervention; Questionnaire Administration; Tailored Intervention
Conditions: Lymphoma; Malignant Solid Neoplasm
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- PRACTICE CRITERIA: Participating practice clusters will be required to identify one (or more) oncologist and/or advanced practice practitioner (APPs; i.e., nurse practitioners, or physician assistants) as part of study eligibility. If another clinician is interested in participating, please contact University of Rochester Cancer Center (URCC) National Cancer Institute Community Oncology Research Program (NCORP) Research Base (RB) for approval
- Oncologists/APPs/other clinicians must be licensed to practice
- Oncologists/APPs/other clinicians must not have a plan to leave or retire from the NCORP practice within one year of enrolling into the study
- PRACTICE CRITERIA: Support/buy-in from oncology physicians and/or APPs and/or other clinicians who are willing to participate in training and study procedures and enroll cancer survivors
- ENTRY CRITERIA FOR ONCOLOGY PHYSICIANS/APPS/OTHER CLINICIANS: Oncology physicians/APPs/other clinicians must work at a participating site with no plans to leave that practice or retire within one year of enrollment into the study. We do not require that any or all oncology physicians and/or APPs at a practice setting agree to participate. Only one clinician is required for the practice cluster to be eligible. If another clinician (other than oncology physician or APP) is interested in participating, please contact URCC NCORP RB for approval
- CANCER SURVIVORS: 65 years or older
- CANCER SURVIVORS: Have completed or will have completed curative-intent treatment (e.g., surgery, chemotherapy, chemotherapy with radiation) for any solid tumor or lymphoma malignancy in last 6 months. If the survivor is receiving curative-intent chemotherapy, run-in study procedures can occur during the last 6 weeks of chemotherapy.
- Cancer survivors who will receive or are receiving other treatments (e.g., hormonal treatment, monoclonal antibodies, immunotherapy, radiation) are eligible
- For patients receiving neoadjuvant chemotherapy for curative intent, the run-in and baseline procedures can occur before or after surgery. Patients should be enrolled within 6 months from the end of surgery
- CANCER SURVIVORS: Be willing and able to come in for study visits or willing to undergo informed consent and assessments remotely via tele-health visits
- CANCER SURVIVORS: Be willing and able to provide informed consent and must sign consent in-person or remotely if it is not convenient or feasible to provide informed consent in-person
- CANCER SURVIVORS: Speak and understand English and/or Spanish. Spanish-speaking cancer survivors are eligible as long as there are appropriate resources in place for completion of study procedures at the practice site. Registration for Spanish-speaking cancer survivors must be approved by the URCC NCORP Research Base after a phone call to determine the feasibility for the practice to enroll a Spanish-speaking participant
- CAREGIVERS: 18 years or older
- CAREGIVERS: Selected by the cancer survivor when asked if there is a "family member, partner, friend or caregiver (age 18 years or older) with whom you discuss or who can be helpful in health-related matters." A caregiver need not be someone who lives with the cancer survivor or provides direct hands-on care
- CAREGIVERS: Speak and understand English and/or Spanish. Spanish-speaking caregivers are eligible as long as there are appropriate resources in place for completion of study procedures. Registration for Spanish-speaking caregivers must be approved by the URCC NCORP Research Base after a phone call to determine the feasibility for the practice to enroll a Spanish-speaking participant
Exclusion Criteria
- CANCER SURVIVORS: Have a condition that precludes their ability to participate in informed consent or procedures (e.g., dementia)
- CAREGIVERS: Caregivers unable to understand the informed consent form or study procedures due to cognitive, health, or sensory impairment will be excluded
- Capacity to conduct informed consent procedures and study procedures will be determined by the coordinators in collaboration with the cancer survivors' oncologists. These procedures are similar to that of URCC 13070, which enrolled caregivers of older patients with advanced cancer
Recruiting US locations
Lewis and Faye Manderson Cancer Center
Tuscaloosa, AL 35401
Site contact: Site Public Contact · 800-338-2948
Kaiser Permanente-Fremont
Fremont, CA 94538
Site contact: Site Public Contact · 877-642-4691 · Kpoct@kp.org
Kaiser Permanente-San Francisco
San Francisco, CA 94115
Site contact: Site Public Contact · 877-642-4691 · Kpoct@kp.org
Helen F Graham Cancer Center
Newark, DE 19713
Site contact: Site Public Contact · 302-623-4450 · lbarone@christianacare.org
Medical Oncology Hematology Consultants PA
Newark, DE 19713
Site contact: Site Public Contact · 302-623-4450 · lbarone@christianacare.org
Hawaii Cancer Care Inc - Waterfront Plaza
Honolulu, HI 96813
Site contact: Site Public Contact · 808-524-6115 · i.webster@hawaiicancercare.com
Straub Clinic and Hospital
Honolulu, HI 96813
Site contact: Site Public Contact · 808-522-4333
Kapiolani Medical Center for Women and Children
Honolulu, HI 96826
Site contact: Site Public Contact · 808-983-6090
Tripler Army Medical Center
Honolulu, HI 96859
Site contact: Site Public Contact · 808-433-6336
Hawaii Cancer Care - Westridge
‘Aiea, HI 96701
Site contact: Site Public Contact · 808-539-2273 · info@hawaiicancercare.com
Pali Momi Medical Center
‘Aiea, HI 96701
Site contact: Site Public Contact · 808-486-6000
OSF Saint Anthony's Health Center
Alton, IL 62002
Site contact: Site Public Contact · 618-463-5623
Fairview Southdale Hospital
Edina, MN 55435
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Hennepin County Medical Center
Minneapolis, MN 55415
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Monticello Cancer Center
Monticello, MN 55362
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Park Nicollet Clinic - Saint Louis Park
Saint Louis Park, MN 55416
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Regions Hospital
Saint Paul, MN 55101
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Lakeview Hospital
Stillwater, MN 55082
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Rice Memorial Hospital
Willmar, MN 56201
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Minnesota Oncology Hematology PA-Woodbury
Woodbury, MN 55125
Site contact: Site Public Contact · 952-993-1517 · mmcorc@healthpartners.com
Lake Regional Hospital
Osage Beach, MO 65065
Site contact: Site Public Contact · 573-302-2768 · clinicaltrials@lakeregional.com
Noyes Memorial Hospital/Myers Cancer Center
Dansville, NY 14437
Site contact: Site Public Contact · WCICTOresearch@urmc.rochester.edu
Northwell Health/Center for Advanced Medicine
Lake Success, NY 11042
Site contact: Site Public Contact · 516-734-8896
Highland Hospital
Rochester, NY 14620
Site contact: Site Public Contact · 585-341-8113
Pluta Cancer Center
Rochester, NY 14623
Site contact: Site Public Contact · 888-823-5923 · ctsucontact@westat.com
University of Rochester
Rochester, NY 14642
Site contact: Site Public Contact · 585-275-5830
Wilmot Cancer Institute at Webster
Webster, NY 14580
Site contact: Site Public Contact · WCICTOresearch@urmc.rochester.edu
Novant Health Breast Surgery - Greensboro
Greensboro, NC 27403
Site contact: Site Public Contact · 336-718-8335 · pjordan@novanthealth.org
Novant Health Cancer Institute - Kernersville
Kernersville, NC 27284
Site contact: Site Public Contact · 336-718-8335 · asmarrs@novanthealth.org
Novant Health Cancer Institute - Mount Airy
Mount Airy, NC 27030
Site contact: Site Public Contact · 336-718-8335 · asmarrs@novanthealth.org
Novant Health Cancer Institute - Statesville
Stateville, NC 28625
Site contact: Site Public Contact · 336-718-8335 · pjordan@novanthealth.org
Novant Health Cancer Institute - Thomasville
Thomasville, NC 27360
Site contact: Site Public Contact · 336-718-8335 · pjordan@novanthealth.org
Novant Health Forsyth Medical Center
Winston-Salem, NC 27103
Site contact: Site Public Contact · 336-718-8335 · pjordan@novanthealth.org
South Central Medical and Resource Center
Lindsay, OK 73052
Site contact: Site Public Contact · 405-756-1414
Geisinger Medical Center
Danville, PA 17822
Site contact: Site Public Contact · 570-271-5251 · HemonCCTrials@geisinger.edu
Geisinger Cancer Center Dickson City
Dickson City, PA 18519
Site contact: Site Public Contact · 877-204-6081 · hemoncctrials@geisinger.edu
Community Medical Center
Scranton, PA 18510
Site contact: Site Public Contact · 570-703-4768 · HemonCCTrials@geisinger.edu
Geisinger Wyoming Valley/Henry Cancer Center
Wilkes-Barre, PA 18711
Site contact: Site Public Contact · 570-271-5251 · HemonCCTrials@geisinger.edu
Chesapeake Regional Medical Center
Chesapeake, VA 23320
Site contact: Site Public Contact · CancerCare@ChesapeakeRegional.com
ThedaCare Regional Cancer Center
Appleton, WI 54911
Site contact: Site Public Contact · 920-364-3604 · ResearchDept@thedacare.org
Saint Vincent Hospital Cancer Center Green Bay
Green Bay, WI 54301
Site contact: Site Public Contact · 920-433-8889 · WI_research_admin@hshs.org
Saint Vincent Hospital Cancer Center at Saint Mary's
Green Bay, WI 54303
Site contact: Site Public Contact · 920-433-8889 · wi_research_admin@hshs.org
Marshfield Medical Center-River Region at Stevens Point
Stevens Point, WI 54482
Site contact: Site Public Contact · 800-782-8581 · oncology.clinical.trials@marshfieldresearch.org
Marshfield Medical Center - Weston
Weston, WI 54476
Site contact: Site Public Contact · 800-782-8581 · oncology.clinical.trials@marshfieldresearch.org
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