Diabetes Treatment in Rural Guatemala
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03626909 |
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Recruitment Status :
Completed
First Posted : August 13, 2018
Last Update Posted : December 24, 2020
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| Condition or disease | Intervention/treatment |
|---|---|
| Diabetes | Other: Primary visit and assessment Other: Follow up visits Other: 3 month visits Other: Unscheduled visits |
Show detailed description
| Study Type : | Observational |
| Actual Enrollment : | 89 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Diabetes Treatment in Rural Guatemala |
| Actual Study Start Date : | January 14, 2018 |
| Actual Primary Completion Date : | December 31, 2019 |
| Actual Study Completion Date : | December 31, 2019 |
- Other: Primary visit and assessment
At the initial visit on entry into the program CHW will collect information and the application will guide initial treatment and referral recommendations. At this visit:
Collection of demographic information and relevant past medical history Medication history, adherence and side effects Glycemic testing, vital signs, and other anthropometric data. Screening for possible complications of diabetes Recommendations for referrals Medication recommendations and counseling
- Other: Follow up visits
CHWs will meet with patients once per month to follow up on adherence and tolerance to medications, assess glycemic control, assess for complications of diabetes, refill medications (with dosing adjustments as needed for side effects, non-adherence or poor glycemic control), and provide diabetic education. These monthly visits will be facilitated by the smartphone application monthly protocol
- Other: 3 month visits
At every 3rd monthly visit, starting with the visit 3 months after enrollment, A1c will be assessed. When A1c is checked, the month 3 medication titration algorithm, is used rather than the monthly titration algorithm, which uses blood glucose. Other than checking A1c and using the A1c-based algorithm as indicated, the procedures performed at the month 3 visit are identical to those of the monthly visit.
- Other: Unscheduled visits
The CHWs live in the same communities as the patients they will be serving. As such, the investigators recognize that patients may come to them with concerns outside of the structure of monthly visits as described above. The investigators have designed an additional module for the smartphone application that guides the CHWs through an assessment for hypoglycemia or severe hyperglycemia and possible complications of diabetes. If a patient or CHW has a concern outside of the scope of these protocols, the CHW will contact a CHW coordinator and/or the medical director for guidance
- Change in HgbA1c [ Time Frame: 3,6,9 and 12 months ]Change in mean percent of HgbA1c compared to value at baseline.
- Patients meeting their HgbA1c treatment goal [ Time Frame: 3,6,9 and 12 months ]Percentage of patients meeting treatment goal for HgbA1c compared to this percentage at baseline. Treatment goal will be A1c ≤7 for most patients, A1c ≤8 for patients age 65 or older or who have 2 or more comorbidities, or other individualized goal for select patients as determined by the medical director
- Fasting blood glucose [ Time Frame: 3, 6, 9 and 12 months ]Mean fasting blood glucose compared to baseline value
- BMI [ Time Frame: 3,6,9 and 12 months ]Body mass index compared to baseline value
- Waist circumference [ Time Frame: 3,6,9 and 12 months ]Waist circumference compared to baseline value
- Blood pressure [ Time Frame: 3,6,9 and 12 months ]Mean systolic and mean arterial pressure compared to baseline value
- Diabetic complications [ Time Frame: 3,6,9 and 12 months ]Number and percentage of patients identified as potentially having the following complications: Angina,foot ulcers,eye complications,hypertension
- Referrals for more advanced care [ Time Frame: 3,6,9 and 12 months ]Number of patients referred for potential complications, poor glycemic control or intolerance of diabetic medications and the number who complete referral
- Medication adverse effects [ Time Frame: Through study completion, an average of 1 year ]Prevalence of adverse effects of metformin and hypoglycemia symptoms
- Medication adherence [ Time Frame: Through study completion, an average of 1 year ]Patient adherence with medication regime
- Community Health Worker adherence [ Time Frame: 3,6,9 and 12 months ]Community health worker adherence to recommendations provided by the application
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Willing to provide written informed consent
- Willing to comply with all study procedures and be available for the duration of the study
- Male or female, at least 18 years of age
- Prior diagnosis of type 2 diabetes
- Resident of one of the rural communities served by the CHW network of San Lucas Tolimán, Guatemala
Exclusion Criteria:
- Type 1 diabetes
- Women who are pregnant
- Current use of insulin
- Renal insufficiency (eGRF <30 mL/min/1.73 m2)
- Unable to provide informed consent -
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03626909
| Guatemala | |
| Hospital Obras Sociales | |
| San Lucas Tolimán, Solala, Guatemala | |
| Principal Investigator: | James Svenson, MD, MS | University of Wisconsin, Madison |
Documents provided by University of Wisconsin, Madison:
| Responsible Party: | University of Wisconsin, Madison |
| ClinicalTrials.gov Identifier: | NCT03626909 |
| Other Study ID Numbers: |
2017-0596 A534100 ( Other Identifier: UW Madison ) SMPH\EMERG MED\EMER MED ( Other Identifier: UW Madison ) |
| First Posted: | August 13, 2018 Key Record Dates |
| Last Update Posted: | December 24, 2020 |
| Last Verified: | December 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Diabetes Mellitus Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases |

