MedPath

The Smart-phone as a Physical Fitness Monitor - Validity, Sensitivity and Motivation InterWalk

Not Applicable
Completed
Conditions
Type 2 Diabetes
Interventions
Other: Support group
Registration Number
NCT02089477
Lead Sponsor
Laura Staun Valentiner
Brief Summary

Low physical fitness may cause several life style related diseases e.g. cardiovascular disease, cancer and type 2 diabetes. It is important to develop reliable methods for measurement which can be used to follow the development of the physical shape both on an individual level and on at population level.

Associated with the development of new training method known as Interval Walking we developed an application for smartphones. The use of the application InterWalk was meant to increase physical activity in patients with type 2 diabetes. The application should both be able to, 1) be a personal trainer when doing interval walking, and 2) measure the individual physical fitness performed as a walking test. The latter function was developed to make the training more personal and individal adapted, so that the training was neither too hard or too easy.

It is necessary to test the walking test against a golden standard for measuring physical fitness and that the test in the application is able to measure and register changes in physical fitness.

Our hypothesis is that the individual test, in the InterWalk Application is reliable and able to register changes in physical fitness in patients with type 2 diabetes. The purpose of this project is investigate the reliability of a smartphone-based test of physical fitness, and to investigate whether the test is able to register changes in physical fitness during the project time (3 month). A secondary aim is to investigate whether individual support during the training period, affect the individual effort and time of interval walking per week.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
37
Inclusion Criteria
  • Type 2 diabetes, age 30-80 y, BMI >18 but <40 kg/m2 and confirmed T2D diagnose
Exclusion Criteria
  • Pregnancy, smoking, contraindication to increased levels of physical activity, insulin dependence, evidence of thyroid, liver, lung, heart or kidney disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SupportSupport groupThe participants in the intervention group receives the intervention and support consisting of: 1. Individual Goal Setting: 2-3 functional goals related to everyday life evaluated every 4th week. 2. SMS send every Sunday with 5 possible responses. depending on the answer of the participant it will cause a telephone call from a project about motivation and barriers for interval walking.
Primary Outcome Measures
NameTimeMethod
The primary outcome is amount of time duing interval walking (in minuts) with InterWalk per week after 3 monthup to 3 months after enrollment
Secondary Outcome Measures
NameTimeMethod
VO2-peek test in the InterWalk Application3 months after enrollment
Quality of data with VO2-peek test in the InterWalk Application3 months after enrollment

quantity of minuts with high and low intervals after 3 month

Frequency of Interval walking with InterWalk3 months after enrollment
validation of InterWalk, VO2-peek test3 months after enrollment

Trial Locations

Locations (1)

Center of Inflammation and Metabolism

🇩🇰

Copenhagen, Denmark

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