Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This study will determine whether Home Telehealth-based implementation of an evidence-based intervention targeting Veterans with persistent poorly-controlled diabetes can improve hemoglobin A1c, patient self-management, and comorbid depressive symptoms in this high-risk, high-cost population. If effective, this intervention (Advanced Comprehensive Diabetes Care) offers a feasible, sustainable, and generalizable approach to managing Veterans with persistent poorly-controlled diabetes, which can be implemented using only existing Home Telehealth services.
Background: Although efforts by VA providers and researchers have improved diabetes care quality for Veterans, individuals with persistent poorly-controlled diabetes mellitus (type 1 or type 2 diabetes with hemoglobin A1c >9.0% for > 1 year despite receipt of medical care) have proven refractory to these widespread improvements, and remain at high risk for complications and accrued costs. Prior research has illustrated that medication regimen complexity, suboptimal self-care, and comorbid depressive symptoms interact to perpetuate suboptimal control among individuals with PPDM. Current models of clinic-based diabetes care do not meet these Veterans' needs. Without the implementation of care delivery strategies that target this population's unique barriers to improved diabetes control, these Veterans will continue to be left behind by progress in diabetes management throughout VA, and will remain at high risk for complications and high costs. We propose using existing local Home Telehealth services to implement Advanced Comprehensive Diabetes Care, a patient-centered, evidence-based intervention combining medication management, self-care behavior support, and depressive symptom management to Veterans with PPDM.
Objectives: The specific aims of this RRP are to: 1) evaluate the effectiveness of the Advanced Comprehensive Diabetes Care among Veterans with persistent poorly-controlled diabetes; 2) utilize a mixed method formative evaluation to assess our main implementation strategy, the use of existing Home Telehealth services to administer the intervention; and 3) generate data we will use to refine local intervention implementation and inform the development of an SDP proposal evaluating broader implementation of the Advanced Comprehensive Diabetes Care intervention.
Methods: We propose a pilot Effectiveness-Implementation Hybrid trial to study the Advanced Comprehensive Diabetes Care intervention in Veterans with persistent poorly-controlled diabetes. After baseline evaluation, 50 Veterans will be randomly assigned into intervention (n = 25) or control groups (n = 25). Veterans randomized to the intervention will be enrolled in the Home Telehealth program at Durham VAMC and will receive the study intervention (telehealth-based medication management, self-care behavior support, and depressive symptom management) for 6 months. Intervention-group Veterans with no depression on baseline assessment will not initially receive the depressive symptom management component, but will be monitored for new symptoms throughout the study. Veterans randomized to the control arm will receive diabetes educational materials and management per their primary provider. The primary effectiveness outcome for this study will be hemoglobin A1c. Secondary effectiveness outcomes will include measures of diabetes self-care, self-reported medication adherence, and depressive symptoms. This RRP will also include a mixed method formative evaluation to qualitatively and quantitatively assess patient-level, provider-level, and organizational barriers and facilitators influencing intervention implementation. Formative evaluation data will be analyzed during the study to consider whether adjustments to the intervention or its implementation may be indicated, and findings will also be used to inform future implementation efforts.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Control | No Intervention | Veterans will receive diabetes educational materials and management per their primary provider | |
| Intervention | Experimental | Veterans randomized to the intervention arm will be enrolled in the HT program, provided with standard telemonitoring equipment by HT nursing staff (current HT practice at DVAMC is use of the Health Buddy 3 device for patients with landline phones and the Cardiocom Interactive Voice Response System for patients with cell phones), and will receive the study intervention for 6 months. Veterans without depressive symptoms on baseline PHQ-9 assessment (PHQ-9 < 10) will not initially be entered into the depressive symptom management component of the intervention, but will be monitored for new symptoms throughout the intervention. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Home Telehealth with Behavioral Education Component | Behavioral | The primary effectiveness outcome for this study will be hemoglobin A1c. Secondary effectiveness outcomes will include measures of diabetes self-care, self-reported medication adherence, and depressive symptoms. |
| Measure | Description | Time Frame |
|---|---|---|
| Diabetes Control | Hemoglobin A1c as measured at baseline, 3m, 6m | Baseline, 3months, 6months |
| Measure | Description | Time Frame |
|---|---|---|
| Diabetes Self Care | Self-Care Inventory-revised as measured at baseline, 3 months, 6 months | Baseline, 3m, 6m |
| Self-reported Medication Adherence | Change in Self-Reported Medication- Taking Scale as measured at baseline, 3 months, 6 months |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Exclusion criteria will include lack of telephone access or severe hearing/ speech impairment that would limit:
Due to challenges with dose adjustment by phone, Veterans on continuous subcutaneous insulin infusion (insulin pumps) will not be eligible for this study.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Matthew J Crowley, MD | Durham VA Medical Center, Durham, NC | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Durham VA Medical Center, Durham, NC | Durham | North Carolina | 27705 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 26540163 | Derived | Crowley MJ, Edelman D, McAndrew AT, Kistler S, Danus S, Webb JA, Zanga J, Sanders LL, Coffman CJ, Jackson GL, Bosworth HB. Practical Telemedicine for Veterans with Persistently Poor Diabetes Control: A Randomized Pilot Trial. Telemed J E Health. 2016 May;22(5):376-84. doi: 10.1089/tmj.2015.0145. Epub 2015 Nov 5. |
Not provided
Not provided
Not provided
Recruitment occurred December 2013-May 2014 at the Durham VA Medical Center outpatient primary care clinics.
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | Control | Veterans will receive diabetes educational materials and management per their primary provider |
| FG001 | Intervention | Veterans randomized to the intervention arm will be enrolled in the HT program, provided with standard telemonitoring equipment by HT nursing staff (current HT practice at DVAMC is use of the Health Buddy 3 device for patients with landline phones and the Cardiocom Interactive Voice Response System for patients with cell phones), and will receive the study intervention for 6 months. Veterans without depressive symptoms on baseline PHQ-9 assessment (PHQ-9 < 10) will not initially be entered into the depressive symptom management component of the intervention, but will be monitored for new symptoms throughout the intervention. Home Telehealth with Behavioral Education Component: The primary effectiveness outcome for this study will be hemoglobin A1c. Secondary effectiveness outcomes will include measures of diabetes self-care, self-reported medication adherence, and depressive symptoms. |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
Not provided
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Control | Veterans will receive diabetes educational materials and management per their primary provider |
| BG001 | Intervention | Veterans randomized to the intervention arm will be enrolled in the HT program, provided with standard telemonitoring equipment by HT nursing staff (current HT practice at DVAMC is use of the Health Buddy 3 device for patients with landline phones and the Cardiocom Interactive Voice Response System for patients with cell phones), and will receive the study intervention for 6 months. Veterans without depressive symptoms on baseline PHQ-9 assessment (PHQ-9 < 10) will not initially be entered into the depressive symptom management component of the intervention, but will be monitored for new symptoms throughout the intervention. Home Telehealth with Behavioral Education Component: The primary effectiveness outcome for this study will be hemoglobin A1c. Secondary effectiveness outcomes will include measures of diabetes self-care, self-reported medication adherence, and depressive symptoms. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Diabetes Control | Hemoglobin A1c as measured at baseline, 3m, 6m | Posted | Mean | Standard Deviation | percentage of glycosylated hemoglobin | Baseline, 3months, 6months |
|
Adverse event data were collected at 3 and 6 months for all participants. Participants randomized to the intervention arm were monitored on a more frequent basis during the intervention telephone contacts.
Patients were asked about recent health events and the medical records were reviewed at each follow-up assessment (3&6mths). Participants participating in the intervention were monitored via the home telehealth equipment and intervention telephone contacts.
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Control | Veterans will receive diabetes educational materials and management per their primary provider |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Hospitalization | Cardiac disorders | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Biopsy | Endocrine disorders | Systematic Assessment | Thyroid nodule |
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr Matthew J Crowley | Durham Veterans Affairs Medical Center | 919-286-6936 | matthew.crowley@va.gov |
Not provided
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D003863 | Depression |
| ID | Term |
|---|---|
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Baseline, 3m, 6m |
| Depressive Symptoms | Change in Patient Health Questionnaire as measured at Baseline, 3 months, 6 months | Baseline, 3m, 6m |
| Transfered care |
|
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
|
|
|
| Secondary | Diabetes Self Care | Self-Care Inventory-revised as measured at baseline, 3 months, 6 months | Posted | Mean | Standard Deviation | units on a scale | Baseline, 3m, 6m |
|
|
|
|
| Secondary | Self-reported Medication Adherence | Change in Self-Reported Medication- Taking Scale as measured at baseline, 3 months, 6 months | Posted | Number | participants | Baseline, 3m, 6m |
|
|
|
|
| Secondary | Depressive Symptoms | Change in Patient Health Questionnaire as measured at Baseline, 3 months, 6 months | Posted | Mean | Standard Deviation | units on a scale | Baseline, 3m, 6m |
|
|
|
|
| 4 |
| 25 |
| 12 |
| 25 |
| EG001 | Intervention | Veterans randomized to the intervention arm will be enrolled in the HT program, provided with standard telemonitoring equipment by HT nursing staff (current HT practice at DVAMC is use of the Health Buddy 3 device for patients with landline phones and the Cardiocom Interactive Voice Response System for patients with cell phones), and will receive the study intervention for 6 months. Veterans without depressive symptoms on baseline PHQ-9 assessment (PHQ-9 < 10) will not initially be entered into the depressive symptom management component of the intervention, but will be monitored for new symptoms throughout the intervention. Home Telehealth with Behavioral Education Component: The primary effectiveness outcome for this study will be hemoglobin A1c. Secondary effectiveness outcomes will include measures of diabetes self-care, self-reported medication adherence, and depressive symptoms. | 3 | 25 | 14 | 25 |
| Hospitalization | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| Hospitalization | General disorders | Systematic Assessment |
|
| Hospitalization | Renal and urinary disorders | Systematic Assessment |
|
| Outpatient Diagnosis | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| Hospitalization | Psychiatric disorders | Systematic Assessment |
|
| Psychiatric Disorder | Psychiatric disorders | Systematic Assessment | Emergency Room Visit |
|
| Hypoglycemia Requiring Asssistance | Investigations | Systematic Assessment |
|
| Biopsy | Skin and subcutaneous tissue disorders | Systematic Assessment | Skin biopsy |
|
| Ear infection | Ear and labyrinth disorders | Systematic Assessment | Emergency Room Visit |
|
| Hyperglycemia | Endocrine disorders | Systematic Assessment | Emergency Room Visit |
|
| Eye pain | Eye disorders | Systematic Assessment | Emergency Room Visit |
|
| Emergency Room Visit | General disorders | Systematic Assessment | We collected adverse events by organ system and categorized them using the Emergency Room distinction. Affected patients may have visited the ER for a range of conditions (for instance pain, cuts, medication refills, etc) |
|
| Emergency Room Visit | Infections and infestations | Systematic Assessment | We collected adverse events by organ system and categorized them using the Emergency Room distinction. Affected patients may have visited the ER for a range of conditions (for instance coughs, illnesses, etc) |
|
| Emergency Room Visit | Musculoskeletal and connective tissue disorders | Systematic Assessment | We collected adverse events by organ system and categorized them using the Emergency Room distinction. Affected patients may have visited the ER for a range of conditions (for instance pain, etc) |
|
| Psychiatric Disorder | Psychiatric disorders | Systematic Assessment | Emergency Room Visit |
|
| Emergency Room Visit | Renal and urinary disorders | Systematic Assessment | We collected adverse events by organ system and categorized them using the Emergency Room distinction. Affected patients may have visited the ER for a range of conditions (for instance pain associated with stones, etc) |
|
| Emergency Room Visit | Respiratory, thoracic and mediastinal disorders | Systematic Assessment | We collected adverse events by organ system and categorized them using the Emergency Room distinction. Affected patients may have visited the ER for a range of conditions (for instance cough, etc) |
|
| cellulitis | Skin and subcutaneous tissue disorders | Systematic Assessment | Emergency Room Visit |
|
| Emergency Room Visit | Vascular disorders | Systematic Assessment | We collected adverse events by organ system and categorized them using the Emergency Room distinction. Affected patients may have visited the ER for a range of conditions (for instance swelling, bleeding, etc) |
|
| Planned Surgery and Proceedures | Surgical and medical procedures | Systematic Assessment |
|
| # Pts with >5 BG Values <70 mg/dL from 1st encounter to end of study | Investigations | Systematic Assessment | Telehealth reported data (intervention group only)- |
|
Not provided
Not provided
Not provided
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
| 6 months |
|
| Mixed Models Analysis |
| 0.027 |
| Mean Difference (Net) |
| 7.7 |
| 2-Sided |
| 95 |
| 0.9 |
| 14.4 |
| No |
| Superiority or Other |
| 6 months |
|
| 0.970 |
| Odds Ratio (OR) |
| 1.02 |
| 2-Sided |
| 95 |
| 0.33 |
| 3.19 |
| No |
| Superiority or Other |
| 6 months |
|
Comparison at 6 months. Scale is 0-27 where a lower score is a better outcome, values were dichotomized to indicate whether or not the patient was depressed.
| Mixed Models Analysis |
| 0.397 |
| Mean Difference (Net) |
| 1.1 |
| 2-Sided |
| 95 |
| -1.4 |
| 3.6 |
| No |
| Superiority or Other |