We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

ASUKI Step Pedometer Worksite Intervention (ASUKI-Step)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01537939
First Posted: February 23, 2012
Last Update Posted: February 23, 2012
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:
Karolinska Institutet
Information provided by (Responsible Party):
Barbara E. Ainsworth, Arizona State University
  Purpose

ASUKI Step is designed to increase the number of days employees walk 10,000 steps and to reduce the number of days employees spend being inactive.

Study aims were:

  1. to have a minimum of 400 employee participants from each university site reach a level of 10, 000 steps per day on at least 100 days (3.5 months) during the trial period;
  2. to have 70% of the employee participants from each university site maintain two or fewer inactive days per week, defined as a level of less than 3,000 steps per day;
  3. to describe the socio-demographic, psychosocial, environmental and health-related determinants of success in the intervention; and
  4. to evaluate the effects of a pedometer-based walking intervention in a university setting on changes in self-perceived health and stress level, sleep patterns, anthropometric measures and fitness.

Condition Intervention Phase
Physical Activity Behavioral: ASUKI Step Worksite Pedometer Intervention Phase 4

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: ASUKI Step Pedometer Worksite Intervention

Further study details as provided by Barbara E. Ainsworth, Arizona State University:

Primary Outcome Measures:
  • Percent of sample walking 10,000 steps per day on at least 100 days (3.5 months) during the trial period. [ Time Frame: End of walking intervention at 6 months ]
    Tally of the participants recording 10,000 steps on their pedometer log for 100 days of the 6 month walking intervention.


Secondary Outcome Measures:
  • Changes in self-perceived health and stress level, sleep patterns, anthropometric measures and fitness. [ Time Frame: End of the 6 month walking study ]
    Compare the measures between the first week and the last week of the 6-month intervention study


Enrollment: 2018
Study Start Date: March 2009
Study Completion Date: December 2009
Primary Completion Date: September 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Walking
Quasi-experimental design with one-group, post-test only
Behavioral: ASUKI Step Worksite Pedometer Intervention
The intervention required participants to accumulate 10,000 steps each day for six months, with a 3-month follow-up period. Steps were recorded onto a study-specific website. Participants completed a website-delivered questionnaire four times to identify socio-demographic, health, psychosocial and environmental correlates of study participation. One person from each team at each university location was randomly selected to complete physical fitness testing to determine their anthropometric and cardiovascular health and to wear an accelerometer for one week.
Other Name: Pedometer-monitored daily walking

Detailed Description:
ASUKI Step is a 9-month pedometer-based worksite intervention conducted at the Karolinska Institutet (KI) in Stockholm, Sweden and Arizona State University (ASU) in the greater Phoenix area, Arizona. ASUKI Step used a quasi-experimental design based on the theory of social support. Participants included 2,118 faculty, staff, and graduate students from ASU (n = 712) and KI (n = 1,406) who participated in teams of 3-4 persons. The intervention required participants to accumulate 10,000 steps each day for six months, with a 3-month follow-up period. Steps were recorded onto a study-specific website. Participants completed a website-delivered questionnaire four times to identify socio-demographic, health, psychosocial and environmental correlates of study participation. One person from each team at each university location was randomly selected to complete physical fitness testing to determine their anthropometric and cardiovascular health and to wear an accelerometer for one week. Incentives were given for compliance to the study protocol that included weekly raffles for participation prizes and a grand finale trip to Arizona or Sweden for teams with most days over 10,000 steps.
  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:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Employed at Arizona State University (ASU)or the Karolinska Institute (KI)
  • The ability to read, speak and understand English (ASU only)
  • Not currently pregnant or lactating
  • Free of physical problems that affect the ability to walk, and e) ages 18 and older

Exclusion Criteria:

  • Inability to walk
  • Not employed or a graduate student at ASU or the KI
  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): NCT01537939


Locations
United States, Arizona
Arizona State University and Karolinska Institutet
Phoenix, Arizona, United States, 85142
Sponsors and Collaborators
Arizona State University
Karolinska Institutet
Investigators
Principal Investigator: Barbara E. Ainsworth, Ph.D. Arizona State University
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Barbara E. Ainsworth, Professor, Arizona State University
ClinicalTrials.gov Identifier: NCT01537939     History of Changes
Other Study ID Numbers: ASUKI2009
First Submitted: February 18, 2012
First Posted: February 23, 2012
Last Update Posted: February 23, 2012
Last Verified: February 2012

Keywords provided by Barbara E. Ainsworth, Arizona State University:
Physical Activity
Walking
Pedometer
Body Composition
Aerobic Fitness