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Diabetes Care for Breast Cancer Patients

Not Applicable
Recruiting
Conditions
PreDiabetes
Breast Cancer
Type 2 Diabetes
Interventions
Behavioral: Nurse-practitioner led intervention
Registration Number
NCT05565534
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

The goal of this study is to find a new way to make diabetes care better for patients with breast cancer and diabetes who are currently receiving cancer treatment. We will have two groups, the researchers will decide who is in which group. One group will be working with a nurse who is trained in diabetes care while the other does not. This will allow the investigators to see if having a trained nurse as part of the care team can help improve the care the patients receive.

Detailed Description

The present study aims to develop a stakeholder-engaged nurse practitioner (NP)-led intervention to improve diabetes care for patients with breast cancer and diabetes who are undergoing cancer treatment.

This is a pilot feasibility study, in which we will use a quasi-experimental pre-post design with non-randomized intervention and control groups. In this feasibility study, the investigators will first enroll 38 eligible patients for the control group and collect effectiveness measures at baseline and follow-up (end of chemotherapy or other cancer treatment, \~12 weeks). Through chart review, the investigators will document cancer treatment regimen completion at follow-up. The investigators will then enroll 38 patients for the intervention group, collecting the effectiveness and implementation outcomes at the end of their treatment (\~12 weeks).

The main hypothesis that will be tested in this pilot study is that a nurse practitioner embedded in the oncology team who is trained in diabetes management may successfully manage diabetes during active cancer care for patients undergoing cancer treatment.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
76
Inclusion Criteria
  • Newly diagnosed invasive cancer

  • Plan to receive neo-adjuvant or adjuvant chemotherapy, targeted therapy, hormonal therapy, or radiation at Weill Cornell Medicine (WCM)

    • Age 18+ years
    • Pre-diabetes OR type 2 diabetes. Treatment with antidiabetic medication OR
  • HbA1c greater than or equal to 5.7 OR

  • Random glucose greater than or equal to OR

  • Fasting blood glucose greater than or equal to 100

Exclusion Criteria
  • Patients receiving hospice care
  • Type 1 diabetes

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Nurse-practitioner led intervention groupNurse-practitioner led interventionA nurse practitioner (NP) who is trained in diabetes on the oncology team will help manage diabetes for breast cancer patients undergoing cancer treatments
Primary Outcome Measures
NameTimeMethod
Provider Questionnaire: Self-report of intervention feasibilityImmediately post-intervention at the week 12 follow-up

Questionnaire: Feasibility of Intervention Measure (4 items)

Response Scale:

For each item, respondents can choose a value from 1-5. Scales can be created for the measure by averaging responses for all 4 items for the overall score. The average score range is from 1 to 5 with higher scores indicating that the intervention is very feasible, and lower scores (below 3) indicating the intervention is not feasible.

Provider Questionnaire: Self-report of intervention acceptabilityImmediately post-intervention at the week 12 follow-up

Questionnaire: Acceptability of Intervention Measure (4 items)

Response Scale:

For each item, respondents can choose a value from 1-5. Scales can be created for the measure by averaging responses for all 4 items for the overall score. The average score range is from 1 to 5 with higher scores indicating more favorable attitudes toward the intervention and lower scores (below 3) indicating less favorable attitudes.

Intervention Completion Success Ratio2 years

Only for the interventional group The number of participants who completed intervention divided by the number of participants who enrolled

Data Collection Success Ratio2 years

Number of participants who completed both surveys divided by the number of participants who were enrolled.

Patient Questionnaire: Self-report of intervention acceptabilityImmediately post-intervention at the week 12 follow-up

Questionnaire: Acceptability of Intervention Measure (4 items)

Response Scale:

For each item, respondents can choose a value from 1-5. Scales can be created for the measure by averaging responses for all 4 items for the overall score. The average score range is from 1 to 5 with higher scores indicating more favorable attitudes toward the intervention and lower scores (below 3) indicating less favorable attitudes.

Recruitment Success Ratio2 years

Number of participants recruited divided by the number of participants approached

Patient Questionnaire: Self-report of intervention feasibilityImmediately post-intervention at the week 12 follow-up

Questionnaire: Feasibility of Intervention Measure (4 items)

Response Scale:

For each item, respondents can choose a value from 1-5. Scales can be created for the measure by averaging responses for all 4 items for the overall score. The average score range is from 1 to 5 with higher scores indicating that the intervention is very feasible, and lower scores (below 3) indicating the intervention is not feasible.

Number of in-person, virtual or phone contacts with the NP2 years

This will assess the degree to which the intervention was implemented over the course of the study

Patient Questionnaire: Self-report of intervention appropriatenessImmediately post-intervention at the week 12 follow-up

Questionnaire: Intervention Appropriateness Measure (4 items)

Response Scale:

For each item, respondents can choose a value from 1-5. Scales can be created for the measure by averaging responses for all 4 items for the overall score. The average score range is from 1 to 5 with higher scores indicating the intervention suits their needs well and lower scores (below 3) indicating the intervention does not fit their needs well.

Provider Questionnaire: Self-report of intervention appropriatenessImmediately post-intervention at the week 12 follow-up

Questionnaire: Intervention Appropriateness Measure (4 items)

Response Scale:

For each item, respondents can choose a value from 1-5. Scales can be created for the measure by averaging responses for all 4 items for the overall score. The average score range is from 1 to 5 with higher scores indicating the intervention suits their needs well and lower scores (below 3) indicating the intervention does not fit their needs well.

Ratio of patients who receive a summary document at the end of the intervention2 years

Number of patients who receive a summary document compared to the number of patients who complete the follow-up visit.

Secondary Outcome Measures
NameTimeMethod
Change in Patient Self-report Responses of Diabetes Treatment Satisfaction QuestionnaireFrom baseline to week 12 follow-up visit

Diabetes Treatment Satisfaction Questionnaire (8 items) DTSQ, score 0-36; higher scores reflecting higher satisfaction

Change in Patient Self-report Responses of Neuropathy as Measured By the PRO-CTCAE SurveyFrom baseline to week 12 follow-up visit

PRO-CTCAE: Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events

Neuropathy - PRO-CTCAE (2 items) 0-8 with higher scores representing worse neuropathy

Change in Patient Self-report Responses of Diabetes Distress Scale QuestionnaireFrom baseline to Week 12 follow-up

Diabetes Distress Scale (17 items) A score of "1" indicates a particular item is not a problem or bother for the patient, whereas "6" represents an item is very concerning for the patient. To score, the patient's responses will be summed and then divided by the number of items in that scale. A mean score of 3 or higher (moderate distress) is considered as a level of distress that is above average.

Change in Patient Self-report Responses of the Functional Assessment of Cancer Therapy-Breast QuestionnaireFrom baseline to Week 12 follow-up

Functional Assessment of Cancer Therapy -Breast (44-items) measures quality of life for patients with breast cancer. Total scores range from 0-148 with higher scores representing better quality of life.

Change in number of Hospitalizations Since Cancer DiagnosisFrom baseline to Week 12 follow-up
Number of missed chemotherapy dosesFrom baseline to Week 12 follow-up

# of doses given subtracted from total # planned doses

Number of participants with a Delay in Chemotherapy AdministrationFrom baseline to Week 12 follow-up

# of days chemotherapy infusion was delayed from schedule date

Number of participants with Chemotherapy Dose ReductionsFrom baseline to Week 12 follow-up

From the electronic medical chart: Indication if chemotherapy dose was reduced

Change in Patient Self-report Responses of the Audit of Diabetes Dependent QoL QuestionnaireFrom baseline to Week 12 follow-up

Audit of Diabetes Dependent Quality of life (QoL) (15 items). For each item, respondents provide a score for both "impact" and "importance." Total weighted scores range from -9 to +3. Lower scores reflect poorer quality of life.

Change in number of Emergency Department (ED) Visits Since Cancer DiagnosisFrom baseline to Week 12 follow-up

Trial Locations

Locations (3)

NewYork-Presbyterian Brooklyn Methodist Hospital

🇺🇸

Brooklyn, New York, United States

New York-Presbyterian Queens

🇺🇸

Flushing, New York, United States

Weill Cornell Medicine

🇺🇸

New York, New York, United States

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