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Project ALIVE (A Lifestyle Intervention Via Email)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00607009
First Posted: February 5, 2008
Last Update Posted: February 5, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Centers for Disease Control and Prevention
Information provided by:
Kaiser Permanente
  Purpose
The objective of this study is to test the effectiveness of an email-based diet and physical activity intervention on increasing physical activity and fruit and vegetable consumption and decreasing intake of saturated and trans fats and added sugars.

Condition Intervention
Inactivity Behavioral: ALIVE

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Email-Based Diet and Activity Promotion in Worksites

Further study details as provided by Kaiser Permanente:

Primary Outcome Measures:
  • change in physical activity [ Time Frame: 4 months ]

Secondary Outcome Measures:
  • change in fruits and vegetables [ Time Frame: 4 months ]
  • health-related quality of life [ Time Frame: 4 months ]
  • presentism [ Time Frame: 4 months ]
  • stage of change [ Time Frame: 4 months ]
  • self efficacy [ Time Frame: 4 months ]

Enrollment: 797
Study Start Date: July 2006
Study Completion Date: May 2007
Primary Completion Date: May 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1
received emails
Behavioral: ALIVE
email-based behavioral program
Placebo Comparator: 2
no contact
Behavioral: ALIVE
email-based behavioral program

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   21 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • regional Northern California KP employees

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00607009


Sponsors and Collaborators
Kaiser Permanente
Centers for Disease Control and Prevention
Investigators
Principal Investigator: Barbara Sternfeld, PhD Kaiser Permanente