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OpenTrials
Completed

NCT Number: NCT00178737

Does the Message Matter? Enhancing Adherence in Healthcare Through Persuasive Messages

In this research we propose to develop a comprehensive model to explain how users process persuasive messages. We then propose to experimentally test varying the persuasiveness of message content in various domains, and assess their impact on adherence by both physicians and patients. Finally based on our conceptual model and results from the experimental data we propose to develop preliminary guidelines to assist developers in designing effective messages.

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Study 1

  • Subjects who have an appointment scheduled at HCHD Baytown Health Center

Study 2

  • Subjects who are neonatology physicians (not in training).
  • Subjects must be able to give signed informed consent.

Study 3

  • Any subjects (students or employee) at the University of Texas Health Science Center at Houston.
  • Subjects must be able to give signed informed consent.

Exclusion criteria

  • No specific individual who meets the inclusion criteria will be excluded.

Treatment and study plan

Electronic reminder message

Behavioral

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Registry information

Important dates

Study completion
2006
First posted
Sep 15, 2005
Registry last updated
Feb 19, 2010

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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