Effects of Exercise Therapy and Soft Brace on Knee Osteoarthritis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity College of Northern Denmark

About this trial

The primary aim of the study is to investigate the effects of supervised exercise therapy and education on the immediate response to using a soft knee brace in patients with knee osteoarthritis (OA).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Patients diagnosed with knee OA and assigned to undergo exercise therapy and education

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Exercise therapy and education.

    Other intervention

    Exercise therapy and education, physiotherapy rehab at Aalborg Municipality

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Patients diagnosed with knee OA1 intervention

Trial outcomes

Primary outcomes

1

Pain - Numerical rating scale (NRS)

NRS is the most common pain scale for quantification pain. The respondent selects a whole number on a scale from 0-10, that best reflects the intensity of his/her pain. 0 being no pain, 10 being the worst pain imaginable.

Time frame
6+12 weeks follow-up

Secondary outcomes

1

Y-balance test (YBT)

The YBT test is a test commonly used in clinical practice to investigate functional balance. The YBT is based on the Star Excursion Balance Test and it has been thoroughly researched. Measured with and without the soft knee brace at baseline, after the treatment program and at 12weeks.

Time frame
6+12 weeks follow-up
2

Self-perceived knee stability question

Self-reported by the patients.

Time frame
6+12 weeks follow-up
3

40-meter walk test

A test of walking speed over shirt distances and changing direction during walking

Time frame
6+12 weeks follow-up

Other outcomes

1

Knee injury and Osteoarthritis Outcome Score (KOOS) (continous)

An instrument to assess the patient's opinion about their knee and associated problems. KOOS has been evaluated and compared to other instruments in several studies. Measured at baseline, after the treatment program and at 12weeks.

Time frame
6+12 weeks follow-up
2

Pain manikin

Self-reported pain assessment by the patients.

Time frame
6+12 weeks follow up
3

Likert scale

Self-reported by the patients

Time frame
6+12 weeks follow-up
4

Analgetic pain medication intake

Self-reported by the patients.

Time frame
6+12 weeks follow-up

Sponsors and contacts

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