Try the modernized ClinicalTrials.gov beta website. Learn more about the modernization effort.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Diabetes Treatment in Rural Guatemala

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
Recruitment Status : Completed
First Posted : August 13, 2018
Last Update Posted : December 24, 2020
Sponsor:
Collaborator:
Stanford University
Information provided by (Responsible Party):
University of Wisconsin, Madison

Brief Summary:
In this study, the investigators will be using a smartphone application that the investigators developed to guide community health workers through the clinical assessment of patients with diabetes including collection of demographic data and past medical history, assessment of medication history, adherence, and adverse effects, measurement of glycemic control, screening for complications, medication administration and titration, and patient counseling.

Condition or disease Intervention/treatment
Diabetes Other: Primary visit and assessment Other: Follow up visits Other: 3 month visits Other: Unscheduled visits

Show Show detailed description

Layout table for study information
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

Intervention Details:
  • 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


Primary Outcome Measures :
  1. Change in HgbA1c [ Time Frame: 3,6,9 and 12 months ]
    Change in mean percent of HgbA1c compared to value at baseline.

  2. 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


Secondary Outcome Measures :
  1. Fasting blood glucose [ Time Frame: 3, 6, 9 and 12 months ]
    Mean fasting blood glucose compared to baseline value

  2. BMI [ Time Frame: 3,6,9 and 12 months ]
    Body mass index compared to baseline value

  3. Waist circumference [ Time Frame: 3,6,9 and 12 months ]
    Waist circumference compared to baseline value

  4. Blood pressure [ Time Frame: 3,6,9 and 12 months ]
    Mean systolic and mean arterial pressure compared to baseline value

  5. 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

  6. 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

  7. Medication adverse effects [ Time Frame: Through study completion, an average of 1 year ]
    Prevalence of adverse effects of metformin and hypoglycemia symptoms

  8. Medication adherence [ Time Frame: Through study completion, an average of 1 year ]
    Patient adherence with medication regime

  9. Community Health Worker adherence [ Time Frame: 3,6,9 and 12 months ]
    Community health worker adherence to recommendations provided by the application



Information from the National Library of Medicine

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.


Layout table for eligibility information
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
Study Population
Subjects will include adults 18 years of age and older and will be recruited from the 19 rural villages surrounding San Lucas Tolimán, Guatemala. Treatment of children with diabetes entails greater complexity and is beyond the scope of this program. Though there are no enrollment restrictions based on race or ethnicity, the majority of the people living in these villages are from the Kaqchikel ethnic group, an indigenous Mayan people of the midwestern highlands of Guatemala.
Criteria

Inclusion Criteria:

  1. Willing to provide written informed consent
  2. Willing to comply with all study procedures and be available for the duration of the study
  3. Male or female, at least 18 years of age
  4. Prior diagnosis of type 2 diabetes
  5. Resident of one of the rural communities served by the CHW network of San Lucas Tolimán, Guatemala

Exclusion Criteria:

  1. Type 1 diabetes
  2. Women who are pregnant
  3. Current use of insulin
  4. Renal insufficiency (eGRF <30 mL/min/1.73 m2)
  5. Unable to provide informed consent -

Information from the National Library of Medicine

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


Locations
Layout table for location information
Guatemala
Hospital Obras Sociales
San Lucas Tolimán, Solala, Guatemala
Sponsors and Collaborators
University of Wisconsin, Madison
Stanford University
Investigators
Layout table for investigator information
Principal Investigator: James Svenson, MD, MS University of Wisconsin, Madison
  Study Documents (Full-Text)

Documents provided by University of Wisconsin, Madison:
Publications of Results:
Layout table for additonal information
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

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
Layout table for MeSH terms
Diabetes Mellitus
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases