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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03539237
Other study ID # GAP05/18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 23, 2018
Est. completion date November 28, 2018

Study information

Verified date January 2019
Source University Medicine Greifswald
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study examines the effect of a video-based intensity level demonstration on self-reported physical activity in individuals aged between 40 and 75 years. Aim of the video demonstration is to achieve a better concordance of physical activity reports with accelerometer-based measurements.


Description:

This study examines whether the demonstration of different intensity levels of physical activity by video in the context of a tablet PC (personal computer)-based survey can achieve a higher degree of concordance between self-reported and accelerometer-measured physical activity compared to an assessment without video demonstration. The recruitment of the study participants in the age range between 40 and 75 years takes place in a shopping center in the city Greifswald in Germany.

Informed consent consists of: (i) activity recording over 7 days using an accelerometer, (ii) completion of standardized questionnaires, (iii) participation in a standardized measurement of weight and height as well as waist and hip circumference.

Participants are asked to wear an accelerometer during the day for a period of 7 days. Subsequently, a questionnaire about the frequency, duration and intensity of physical activity in the last 7 days will be answered in the DZHK (Deutsches Zentrum für Herz-Kreislauf-Forschung)- examination center. Prior to the physical activity assessment the study participants are randomly assigned to the study conditions "Video" or "No Video" (ratio 1:1). Optionally, participants may receive feedback on their physical activity measured by accelerometer upon completion of the study.


Recruitment information / eligibility

Status Completed
Enrollment 379
Est. completion date November 28, 2018
Est. primary completion date November 28, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria:

Exclusion Criteria:

- cognitive impairment

- inadequate language skills

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Video demonstration of physical activity intensity levels
In the video demonstration, an approximately 50 year old male explains 1) light-intensity, 2) moderate-intensity, and 3) vigorous-intensity physical activity referring to differences in heart rate, breathing frequency and capability to talk normally. Simultaneously, on a treadmill he demonstrates the body signs of the three intensity levels. He gives examples and points out that there are individual differences in the intensity evaluation of comparable activities.

Locations

Country Name City State
Germany Institute of Social Medicine and Prevention, University Medicine Greifswald Greifswald

Sponsors (2)

Lead Sponsor Collaborator
University Medicine Greifswald Deutsches Zentrum für Herz-Kreislauf-Forschung (DZHK)

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference between physical activity measured by self-report and by accelerometry Measures: assessement via tablet PC (International Physical Activity Questionnaire-Short Form, IPAQ-SF) and objective measurement by accelerometry The accelerometer is worn for 7 days and then the IPAQ-SF is retrospectively answered for these 7 days.
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