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OpenTrials
Completed

NCT Number: NCT02806700

Twitter and Diabetes

Twitter use is surprisingly well represented across broad demographic population segments and health-related messages. The promise of using Twitter is that its use is growing rapidly, it allows the investigators to view communications that were impossible to intercept before, and it potentially provides information faster and less expensively than collection from other media channels. Prior work also supports that social media interventions can improve health behavior change (e.g. weight loss, physical activity) and outcomes.The overarching goals of this proposal are to understand the uses and limitations of this communication channel to improve patients' ability to manage their CV health condition.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

About this study

Use Twitter to deliver high impact CV health related content to improve patient activation and disease management for diabetes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diabetes
  • uses social media

Exclusion criteria

  • <21 years of age
  • pregnant

Treatment and study plan

Twitter Diabetes Intervention

Behavioral

This group will be asked to use twitter for heart health ( e.g. tweeting, following, receiving tweets)

Primary outcomes

  1. 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.

Secondary outcomes

  1. 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.

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Jun 21, 2016
Registry last updated
Oct 21, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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