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A Quality Improvement Approach to the Management of Chronic Lymphocytic Leukemia

A Quality Improvement Approach to the Management of Chronic Lymphocytic Leukemia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02619604
Acronym
Med-IQ CLL
Enrollment
50
Registered
2015-12-02
Start date
2016-05-31
Completion date
2017-02-28
Last updated
2017-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Lymphocytic Leukemia

Brief summary

This project addresses the need to improve physician knowledge and clinical practice patterns related to quality of life (QoL) concerns for patients with chronic lymphocytic leukemia (CLL).

Detailed description

This multifaceted initiative will include evaluating patient perspectives on their QoL, evaluating provider perspectives on managing QoL, and providing education to the whole CLL care team (hematologists/oncologists, nurse practitioners, physician assistants, and nurses) on contemporary approaches for individualized, patient-centered management of CLL. Providers, including physicians, nurse practitioners, and physician assistants will participate in educational initiatives geared towards enhancing their knowledge and confidence with managing QoL concerns for patients with CLL. Pre and post surveys will be conducted with providers to evaluate change in these areas. The project aims to train this team on how to enhance communication with patients and caregivers as a means to increase patient engagement in care and QoL in this population.

Interventions

OTHEREducation Intervention

Education interventions will be delivered sporadically within the 6-month window between the time the clinician completes the pre-survey and when he/she completes the post-survey. Interventions consist of e-brief publications, teleconferences with project faculty, and evidence based resources.

Sponsors

Med-IQ
CollaboratorINDUSTRY
Gilead Sciences
CollaboratorINDUSTRY
Genentech, Inc.
CollaboratorINDUSTRY
Duke University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Clinician * Participant must be a hematologist, oncologist, nurse practitioner, or physician assistant who practices medicine in the Duke Cancer Network * Participant treats patients with CLL * Participant is willing to participate in the educational component of this project Inclusion Criteria: Patient * Patient has a diagnosis of Chronic Lymphocytic Leukemia * Patient is over the age of 18 * Patient is being treated at a Duke Cancer Network affiliate site, * Patient is expected to see their physician or another member of their care team at least 3 times annually. * Signed informed consent

Exclusion criteria

Clinician * None

Design outcomes

Primary

MeasureTime frame
Change in provider knowledge with management of Quality of Life Concerns for CLL patients, as measured by surveyBaseline, 6 months
Change in provider confidence with management of Quality of Life Concerns for CLL patients, as measured by surveyBaseline, 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026