Diabetes Clinical Trial
Official title:
An Innovative Approach With Group Counseling and Mindfulness Training Among Prediabetes Patients
Verified date | December 2020 |
Source | Clemson University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Examining a number of health outcomes in those with diabetes and prediabetes before and after a group-based mindfulness intervention.
Status | Completed |
Enrollment | 19 |
Est. completion date | January 31, 2020 |
Est. primary completion date | January 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years or older - English speaking - Having a diagnosis of diabetes or prediabetes - Participation in a previous group-based clinical care model-JUMP (as in "JUMPing into Diabetes Control") Exclusion Criteria: - Under 18 years old - Non-English Speaking - not having a diagnosis of diabetes or prediabetes - No participation in JUMP model |
Country | Name | City | State |
---|---|---|---|
United States | Prisma Health | Greenville | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Clemson University | Prisma Health-Upstate, University of California, Los Angeles |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Intervention Attendance | How many hours of intervention sessions an individual attended | 8-weeks while completing the intervention | |
Secondary | Perceived Stress Scale | Change in perceived stress measured by 4 Items to assess perceived stress where higher levels indicating higher levels of stress with a range of 4 to 20. | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Depression | Change in depression scores from the Center for Epidemiologic Studies Depression Scale (CES-D), where higher scores indicate higher levels of depression with a range of 0 to 80. | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Anxiety | Change in anxiety assessed using the Generalized anxiety disorder 7-item scale (GAD-7). | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Medication Adherence | Change in medication adherence assessed using the 8-item Morisky Medication Adherence Scale. A higher score indicates higher adherence with a range of 0 to 8. | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Perceived Health Status | Change in perceived health status assessed using a question asking participants to rate their health status on a 5-points rating scale where lower ratings indicate higher levels of perceived health status and higher ratings indicate lower levels of perceived health status. | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Sleep Quality | Change in sleep quality assessed using the Pittsburgh Sleep Quality Index (PSQI) ranges from 7 to 28, with higher scores indicating worse sleep quality. | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Physical Activity | Change in physical activity assessed using the Rapid Assessment of Physical Activity Scale (RAPA). | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Mindfulness | Change in Mindfulness assessed using a 15-item Five-Facet Mindfulness Questionnaire (FFMQ). | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | HbA1C levels | HbA1C blood levels | Up to 3 months before intervention, immediately following intervention, one month after intervention | |
Secondary | Program satisfaction and barriers for attending sessions | Open ended questions to address engagement in the intervention, perceived usefulness of the MBSR, recommendations for intervention modification, what participants enjoyed most/least about the intervention, and reasons for missing intervention sessions. This is a qualitative measure, not numeric values were assigned. Based on Zgierska A, Rabago D, Zuelsdorff M, Coe C, Miller M, Fleming M. Mindfulness meditation for alcohol relapse prevention: a feasibility pilot study. J Addict Med. 2008 Sep;2(3):165-73. doi: 10.1097/ADM.0b013e31816f8546. | Immediately following intervention |
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