Lay Theories of Health in Young and Middle Aged American Adults

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2007 by University of Michigan.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Blue Cross Blue Shield of Michigan Foundation
Information provided by:
University of Michigan
ClinicalTrials.gov Identifier:
NCT00458172
First received: April 4, 2007
Last updated: April 6, 2007
Last verified: March 2007

April 4, 2007
April 6, 2007
April 2007
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Complete list of historical versions of study NCT00458172 on ClinicalTrials.gov Archive Site
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Lay Theories of Health in Young and Middle Aged American Adults
Study 1 of Lay Theories of Health: Conceptualizations of Physical, Mental, and Social Health in Young and Middle-Aged Adults

This study is the second empirical investigation in a series of studies, examining what everyday people believe that it means to be healthy. Part of this research also involves examining whether these lay theories of health vary according to various demographic classifications.

In the journal "Science," Engel (1977) proposed the term "biopsychosocial model" to recognize the social and psychological factors impacting health and illness. Psychologists have played a significant role in contributing to current evidence for this model, including understanding how individuals think about their health.

Work in this area has corresponded to work on the implicit theories of individuals, and how those implicit theories have an impact upon cognition, affect, and behavior. Implicit theories are mental constructions about specific phenomena which, while often elaborate in structure, content, and function, are not well articulated by those who hold them.

A failure to thoroughly investigate lay theories of health has implications for the biopsychosocial model of health and illness, which states that it is not only the knowledge of the physician, but also the beliefs of the patient, that have consequences for the patient’s experience of health and illness. Research on individual beliefs regarding illness has been accumulating for some time, and it is becoming apparent that these beliefs have significant consequences for individual health behavior. However, current studies assessing lay theories regarding illness may be inadequate to achieving the goal of fully learning how lay theories have an impact upon health. The methodologies utilized rarely distinguish whether the implicit theories under study should be attributed to laypeople or to experts, and tend to assume that health and illness have perfect reciprocal correspondence with one another in the minds of laypeople. If researchers hope to understand laypeople’s theories about health, exclusively investigating lay theories of illness will not suffice to answer the question.

The present series of studies seeks to investigate a number of unanswered questions in the existing literature on lay theories of health. In a Prestudy, we investigated how adult laypeople define what it is to be healthy through open-ended survey questions. At the present time (the focus of the current IRB application) we hope to have participants rate the importance of each of the previously-gathered items to their concept of health (Study 1). We will then present the most important items in pairs to a second sample, and ask those participants to rate how similar or dissimilar the items are to one another. From these ratings, we will determine the structure of lay theories of health through scaling procedures. After determining the structure of lay theories (e.g., in terms of dimensions), we will focus on developing a comprehensive measure of lay theories of health. We will at that time conduct a series of validation studies to determine whether and how these dimensions of lay theories differ from those of experts, do or do not correspond with existing constructs measuring well-being, and are utilized by laypeople in making health judgments and decisions (which will be reviewed and conducted at a later date).

Observational
Additional Descriptors: Convenience Sample
Additional Descriptors: Psychosocial
Time Perspective: Cross-Sectional
Time Perspective: Retrospective/Prospective
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Healthy
Behavioral: Assessment of beliefs and attitudes
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
400
July 2007
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Inclusion Criteria:

  • English primary language
  • U.S. residency (but not necessarily citizenship)

Exclusion Criteria:

  • Only by age
Both
18 Years to 50 Years
Yes
Contact: Christina A Downey, M.S. 734-764-6571 clapan@umich.edu
Contact: Edward C Chang, Ph.D. 734-764-6314 changec@umich.edu
United States
 
NCT00458172
HUM00011805
No
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University of Michigan
Blue Cross Blue Shield of Michigan Foundation
Principal Investigator: Christina A Downey, M.S. University of Michigan
University of Michigan
March 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP