- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02806700
Twitter and Diabetes
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- diabetes
- uses social media
Exclusion Criteria:
- <21 years of age
- pregnant
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Twitter Diabetes Control
This group will be identified as having diabetes from Twitter.
This group will be contacted and asked to complete brief surveys
|
|
|
Experimental: Twitter Diabetes Intervention
This group will be identified as having diabetes from Twitter.
This group will be contacted and asked to complete brief surveys.
This group will be asked to use twitter for heart health ( e.g.
tweeting, following, receiving tweets)
|
This group will be asked to use twitter for heart health ( e.g.
tweeting, following, receiving tweets)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Patient Activation Measure (PAM) Score From Baseline
Time Frame: baseline and 6 months
|
The Patient Activation Measure (PAM) is a validated and reliable tool that assesses a person's ability to manage their health, using a 100-point total score scale and four activation levels. The total score ranges from 0 to 100, with higher scores indicating better outcomes-specifically, higher scores represent better outcomes. The overall score is summed from individual items, reflecting the level of activation and self-management ability. The four levels are: Level 1 (Score: 0-47.0): Lowest activation, indicating disengagement and lack of confidence in managing health. Level 2 (Score: 47.1-55.1): Some awareness of self-management but limited skills and confidence. Level 3 (Score: 55.2-67.0): Actively trying to manage health but inconsistent success. Level 4 (Score: 67.1-100): Highest activation, indicating confidence and proactive health management. |
baseline and 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Systolic Blood Pressure From Baseline
Time Frame: baseline and 6 months
|
Initial systolic blood pressure (SBP) measurements were obtained from the electronic medical record (EMR). For the majority of patients, final blood pressure measurements (i.e., the 6-month measurement) were obtained in a five to eight month period after enrollment from a documented reading in the the EMR. For patients who did not have a documented SBP reading in the health system during this time period, we requested that patients either meet our team in person for a manual reading or provide a photograph from their mobile phone of the screen showing their SBP reading from a home blood pressure cuff, pharmacy machine, or doctor's office from outside of our health system. |
baseline and 6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01: HL122457-0IA1
- R01HL122457-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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