The Smart City Active Mobile Phone Intervention (SCAMPI) (SCAMPI)

August 12, 2019 updated by: Marie Löf, docent, Karolinska Institutet

The Smart City Active Mobile Phone Intervention (SCAMPI) Study: a Randomized Controlled Trial to Promote Physical Activity Through Active Transportation

Physical inactivity is still a major public health problem. Active transportation i.e. walking or cycling for transport can contribute to greater total physical activity. The specific aim of this study is to evaluate if a 12-week mobile phone application can increase time spent in active transportation (cycling or walking) and in moderate-to-vigorous physical activity in Swedish adults aged 20-65 years.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

253

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Stockholm, Sweden, 60337
        • Karolinska Institutet

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 20-65 years of age
  • living in Stockholm or its suburbs
  • being able to understand Swedish sufficiently well in order to understand the purpose of the study and the content of the intervention

Exclusion Criteria:

  • having a disease prohibiting them from participation in moderate physical activity such as walking or cycling

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mobile phone based intervention
Participants in the intervention group will receive a 12 week mobile phone based program via a mobile phone application specifically designed for this study. The program will include information, advice and strategies to increase active transportation. Feedback will be provided on personal goals.
Participants will receive supporting messages through a mobile phone based intervention.
No Intervention: Control
No information

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total activity and moderate-to-vigorous physical activity
Time Frame: At the end of the intervention which is 12 weeks after baseline
Accelerometer outputs including time spent in moderate-to-vigorous physical activity
At the end of the intervention which is 12 weeks after baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Walkability
Time Frame: At the end of the intervention which is 12 weeks after baseline
Perception of neighborhood
At the end of the intervention which is 12 weeks after baseline
Active transportation
Time Frame: At the end of intervention which is 12 weeks after baseline
Time spent walking and cycling in minutes per day
At the end of intervention which is 12 weeks after baseline
Total activity and moderate-to-vigorous physical activity
Time Frame: At the six month follow-up
Accelerometer outputs including time spent in moderate-to-vigorous physical activity
At the six month follow-up
Walkability
Time Frame: At the six month follow-up
Perception of neighborhood
At the six month follow-up
Active transportation
Time Frame: At the six month follow-up
Time spent walking and cycling in minutes per day
At the six month follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 18, 2017

Primary Completion (Actual)

June 30, 2019

Study Completion (Actual)

June 30, 2019

Study Registration Dates

First Submitted

March 9, 2017

First Submitted That Met QC Criteria

March 15, 2017

First Posted (Actual)

March 22, 2017

Study Record Updates

Last Update Posted (Actual)

August 13, 2019

Last Update Submitted That Met QC Criteria

August 12, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 2016-00138

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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