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OpenTrials
Completed

NCT Number: NCT00607009

Project ALIVE (A Lifestyle Intervention Via Email)

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.

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Key information

Conditions

Inactivity Behavior Sedentary Behavior

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • regional Northern California KP employees

Exclusion criteria

  • none

Treatment and study plan

ALIVE

Behavioral

ALIVE email-based behavioral program based on the participants selected intervention - physical activity, fats/sugars or fruits/vegetabls

Primary outcomes

  1. change in physical activity

    Time frame: 4 months

Secondary outcomes

  1. change in fruits and vegetables

    Time frame: 4 months

  2. health-related quality of life

    Time frame: 4 months

  3. presentism

    Time frame: 4 months

  4. stage of change

    Time frame: 4 months

  5. self efficacy

    Time frame: 4 months

Sponsors and collaborators

Lead sponsor

Kaiser Permanente

Other

Collaborators

  • Centers for Disease Control and Prevention

Registry information

Official study title

Email-Based Diet and Activity Promotion in Worksites

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
Feb 5, 2008
Registry last updated
Apr 24, 2019

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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