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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05436327
Other study ID # 2021-0881
Secondary ID NCI-2022-05359
Status Recruiting
Phase N/A
First received
Last updated
Start date May 6, 2022
Est. completion date January 31, 2025

Study information

Verified date April 2024
Source M.D. Anderson Cancer Center
Contact Lisa Marie Lowenstein, PhD, MPH
Phone 713-563-0020
Email AgingCancerStudy@mdanderson.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To improve patient-centered outcomes for older patients with cancer considering or receiving chemotherapy and their caregivers. To do this, the project team will (a) establish the effectiveness of GA on communication about age-related concerns, patient and caregiver satisfaction with communication about age-related concerns, quality of life, and patient-reported side effects of chemotherapy; (b) evaluate the success of the implementation strategies on the adoption, reach, and fidelity of implementing the GA in community oncology practices; and (c) identify the resources needed to implement GA and the GA-guided recommendations in community oncology practices for older patients considering or receiving chemotherapy.


Description:

Objectives: - Establish the effectiveness of GA on patient and caregiver satisfaction and communication about age-related concerns for older patients receiving chemotherapy in community oncology practices. - Evaluate the success of our implementation strategies on the reach, adoption, and fidelity of implementing the GA in community oncology practices. - Identify the resources needed to implement GA and the GA-guided recommendations in community oncology practices for older patients receiving chemotherapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date January 31, 2025
Est. primary completion date January 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Practice Staff Participants Inclusion Criteria: - Aged 18 years or older - A practicing clinician (e.g., oncologist, nurse practitioners, physician assistant, advanced practice nurse, registered nurse, medical assistant) or other practice staff (e.g., administrators and IT) - Fluent in English (reading and speaking) - Have access to computer, laptop, tablet, or smart phone Exclusion Criteria: - Have plans to leave the practice in six months (e.g., retiring or changing organizations) - Unable to provide consent Patient Participants Inclusion Criteria: - Aged 65 and older - Considering a new chemotherapy plan Exclusion Criteria: • Have been diagnosed with a health condition that precludes their ability to participate in informed consent or in the intervention (e.g., dementia which limits decision-making capacity). Care Partner/Caregiver Participants (Care partners can be any partner, spouse, family member, and/or friend that has been identified by the patient and/or clinical team that supports the patient through treatment.) Inclusion Criteria: - Aged 18 years and older - Fluent in English (reading and speaking) - Have access to computer, laptop, tablet, or smart phone Exclusion Criteria: • Unable to provide consent Inclusion of Special Populations: Employees. The rationale for including employees is to gain a better understanding of how we can improve cancer care for older patients with cancer receiving chemotherapy. It is possible that some employees may be pregnant women or military personnel. We intend to include these individuals as long as they meet the inclusion and exclusion criteria because this is a clinical improvement project to promote the implementation of the GA in routine clinical practice and should have external validity. These individuals would not be excluded in other clinical improvement projects outside of a research study. Other special populations. This study will not include other special subject populations (students, Non-English-Speaking Populations, Minors, Human Fetuses; Neonates (infants under 30 days old), prisoners/detainees (wards)) because the purpose of the study is to understand the implementation of the GA in clinical oncology practices and its impact on patients 65+ with cancer and their care partners satisfaction with care, communication about their care, quality of life, and patient (65+) reported toxicities.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Geriatric Assessment
Clinical staff receive (a) training in GA and workflow management strategies (<60 minutes) at baseline, (b) monthly facilitation and technical support calls (15-30 minutes) for 12 months, and (c) a group-based quarterly call for 12 months. For 12 months, clinical staff implement GA strategies during visits with older adult (65+) patients planning to receive new chemotherapy regimen and their care partners/caregivers.

Locations

Country Name City State
United States MD Anderson Cancer Center Houston Texas

Sponsors (2)

Lead Sponsor Collaborator
M.D. Anderson Cancer Center Patient-Centered Outcomes Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reach of Geriatric Assessment (GA) implementation in routine medical practice monthly over 12 months of implementation, and 6 months after implementation
Primary Reach of Geriatric Assessment (GA) implementation in routine medical practice as measured by applying the reach formula (# people served divided by potential # of people) to the following four metrics: a) patients per month who received the Geriatric Assessment (GA), b) patients per month who received Geriatric Assessment (GA)-guided recommendations, c) total patients per month age 65+, d) total patients per month who were age 65+ and receiving new chemotherapy or deciding to start chemotherapy. monthly over 12 months of implementation, and 6 months after implementation
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