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Completed

NCT Number: NCT01299883

West Philadelphia Consortium Randomized Control Trial

The investigators will evaluate the effects of an integrated risk counseling program on behavioral and psychological outcomes in African American men and women in a randomized trial that is implemented and evaluated collaboratively through the West Philadelphia Consortium to Address Disparities. The specific aims of this research are as follows:

1. To evaluate the effects of integrated versus disease specific counseling on risk exposure behaviors. The investigators predict that compared to individuals who receive disease specific counseling, those who receive integrated counseling will report greater intake of fruits and vegetables and increased rates of physical activity. 2. To evaluate effects of integrated versus disease specific counseling on psychological outcomes. The investigators predict that compared to individuals who receive disease specific counseling, those who receive integrated counseling will report greater risk comprehension related to cancer and cardiovascular disease and will be more motivated to make behavioral changes. 3. To identify the mechanisms through which integrated risk counseling leads to behavioral change. The investigators predict that changes in risk exposure behaviors (e.g., diet and physical activity) will be mediated by increased risk comprehension and self-efficacy for diet and physical activity.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Pennsylvania Center for Community Based Research and Health Disparities

Philadelphia, Pennsylvania, 19104, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • African American
  • Age 18-75
  • Resident of Philadelphia

Exclusion criteria

  • Previous or current cancer diagnosis
  • Previous or current diagnosis of a CVD
  • Cognitive disorder

Treatment and study plan

Integrated vs Non-integrated Risk Education

Other

Integrated group receives education about risk factors for both cancer and CVD whereas the non-integrated group receives information about CVD only to assess differences in health behavior outcomes.

Primary outcomes

  1. Dietary and physical activity behaviors

    Time frame: 12 months

Secondary outcomes

  1. Exposure to program in terms of attendance

    Time frame: 4 wks.

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Registry information

Official study title

West Philadelphia Consortium to Address Disparities

Important dates

Study start
2008
Primary completion
2017
Study completion
2017
First posted
Feb 18, 2011
Registry last updated
Oct 11, 2017

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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