Diabetes Clinical Trial
— I HEALOfficial title:
Improving Health Engagement and Lifestyle Management for Breast Cancer Survivors With Diabetes
| Verified date | February 2022 |
| Source | Duke University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The proposed randomized clinical trial evaluates a diabetes coping skills training (DCST) intervention for improving breast cancer survivors' abilities to manage symptoms and adhere to recommended diabetes self-management. The telephone-based DCST protocol integrates three key strategies to reduce symptoms and improve diabetes self-management: coping skills training for managing symptoms, adherence skills training, and healthy lifestyle skills training. The investigator will test the effects of the DCST intervention by comparing it to diabetes education alone. Physical symptoms, psychological distress, diabetes self-management behaviors, and self-efficacy for managing symptoms and diabetes self-management will be assessed at baseline and 3, 6, and 12 months. Physical activity (i.e., daily steps and distance) will be assessed using wireless activity trackers and data will be obtained from home blood glucose monitoring devices. Glycosylated hemoglobin (HbA1c) will be assessed at baseline, 6, and 12 months.
| Status | Completed |
| Enrollment | 80 |
| Est. completion date | December 1, 2021 |
| Est. primary completion date | December 1, 2021 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 21 Years and older |
| Eligibility | Inclusion Criteria: - diagnosis of Stage I to III breast cancer, - diagnosis of diabetes mellitus type 2 - completed local definitive treatment (i.e., surgical treatment, chemotherapy and/or radiation therapy), - physician verification of ability to participate in the intervention, - English speaking. Exclusion Criteria: - <21 years of age, - severe cognitive or hearing impairment, - unable to provide meaningful consent (i.e., impairment such that descriptions of the research are not clearly understood), - presence of a health problem that precludes safe participation in the intervention. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Duke University Medical Center | Durham | North Carolina |
| Lead Sponsor | Collaborator |
|---|---|
| Duke University |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in physical symptoms | The Checklist measures the severity of different symptoms (e.g., pain, fatigue, numbness and tingling) associated with illness and disease. | baseline, 3 months, 6 months and 12 months | |
| Primary | Change in psychological distress | The eight-item Patient Reported Outcomes Information System (PROMIS). | baseline, 3 months, 6 months and 12 months | |
| Primary | Change in psychological distress | Anxiety will be assessed using the seven-item GAD-7 Scale. | baseline, 3 months, 6 months and 12 months | |
| Secondary | Accessing change in Diabetes self-management behaviors via self reported medication adherence | Participants who receive DCST will exhibit greater improvements in medication adherence compare to the education group. | Baseline to 12 months | |
| Secondary | Accessing change in Diabetes self-management behavior via Barriers to taking medication | Participants who receive DCST will exhibit greater improvements in medication adherence compare to the education group. | Baseline to 12 months | |
| Secondary | Accessing change in Diabetes self-management behavior via Adherence to diabetes self-management behaviors | Participants who receive DCST will exhibit greater improvements in physical activity, dietary patterns, medication adherence, and adherence to blood glucose monitoring compare to the education group. | Baseline to 12 months | |
| Secondary | Accessing change in Diabetes self-management behavior via Use of home blood glucose monitoring | Participants who receive DCST will exhibit greater improvements in adherence to blood glucose monitoring compare to the education group. | Baseline, 6 months and 12 months | |
| Secondary | Improved glycemic control | Participants who receive DCST will show greater improvements in HbA1c compared to the diabetes education alone. | Baseline, 6 months and 12 months | |
| Secondary | Change in self-efficacy | This contains 5 items that inquire about patients' certainty about degree of pain control, pain during daily activities, controlling pain during sleep, and making pain reductions without extra medication. | Baseline, 6 months and 12 months | |
| Secondary | Change in Physical Activity | Patient-reported physical activity will be assessed using the well-validated Community Healthy Activities Model Program for Seniors (CHAMPS).
Participants who receive DCST will show improved self efficacy for managing symptoms and diabetes self-management compared to the diabetes education alone. |
Baseline, 6 months and 12 months | |
| Secondary | Assessing change in Physical Activity | Wireless activity tracking devices will be used to assess daily steps and distance.
Participants who receive DCST will show improved self efficacy for managing symptoms and diabetes self-management compared to the diabetes education alone. |
Baseline, 6 months and 12 months |
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