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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03125954
Other study ID # InactivityOAIII
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 8, 2017
Est. completion date July 29, 2018

Study information

Verified date December 2018
Source Frederiksberg University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is an objective cohort study using objective recording of physical activity (accelerometry) during and after the GLAiD intervention to investigate if a sedentary behavior change by participating in an 6-week physiotherapy-led exercise and education program (GLAiD) occurs. The GLAiD intervention is an education and exercise based intervention aiming at decreasing pain and improving function in patients with knee osteoarthritis.

The primary outcome is change in objective recorded physical activity between baseline and follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date July 29, 2018
Est. primary completion date July 29, 2018
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- =40 years

- Diagnosed with knee OA

- Willing and able to complete study visits and procedures

- Owner of a smartphone or tablet

- Eligible for participation in the GLAID treatment

- Speaks, reads and writes Danish language

Exclusion Criteria:

- Any condition, which in the opinion of the Investigator, would put the subject at increased safety risk by participation, or otherwise make the subject unsuitable for this study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
standardized exercise treatment for knee OA in Denmark (GLAiD)
objective measurement of physical activity before, during af after the GLAiD intervention

Locations

Country Name City State
Denmark The Parker Institute Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Frederiksberg University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Objectively measured physical activity accelerometer recorded physical activity 6 weeks
Secondary Knee Injury and Osteoarthritis Outcome Score(KOOS) KOOS questionnaire baseline (day 1) and follow-up (after 6 weeks)
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