Clinical Trials Logo

Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01119547
Other study ID # PEPOA-E
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date September 2010
Est. completion date September 2012

Study information

Verified date April 2010
Source Lund University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if inclusion of exercise in an education program for patients with osteoarthritis can improve self efficacy, self-perceived health and function.


Description:

Osteoarthritis (OA) is a degenerative disease, considered to be one of the major national diseases that cause suffering for affected patients and costs for society.The predominant symptoms are pain, stiffness and impaired quality of life, often together with psychological distress. Treatment often consists of medication. Later in the disease, when the joint is destroyed, joint replacement surgery commonly occurs. Physical exercises aimed to increase muscle strength, endurance, proprioception and stability have proved to influence cartilage as well as function, symptoms and quality of life positively. Physical exercise may also reduce the need for hospital care after knee joint replacement.Research suggests that patient education is feasible and valuable in terms of improvements in quality of life, in function, in well-being and improved coping . Accordingly, guidelines recommend education and exercise as a core treatment for osteoarthritis.

Since 1994, Primary Health Care in Malmö has used a patient education programme directed towards OA.The program does not include exercise. In 2007-09 a study was made to investigate this education program.The study showed improvements in self-perceived health and in a few functional tests but not in self-efficacy.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 2012
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Clinical diagnosis of osteoarthritis

Exclusion Criteria:

- Must be able to speak and understand swedish

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise in a group
The patient do their individual exercise program in a group.
Home exercise
The patient exercise their individual program at home during 6 v.

Locations

Country Name City State
Sweden Primary Health Care Malmö Skåne

Sponsors (1)

Lead Sponsor Collaborator
Lund University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Arthritis self-efficacy scale Measure the patients self-efficacy at baseline
Primary One-leg rising from sitting to standing measure the strength at baseline
Primary Grip Ability Test Measure function of the hand at baseline
Primary QuickDash Measure self-percieved function of the arm/hand at baseline
Primary Arthritis self-efficacy scale Measure the patients self-efficacy after 4 month
Primary One leg rising from sitting to standing measure the strength after 4 month
Primary Grip Ability Test Measure function of the hand after 4 month
Primary QuickDash Measure self-percieved function of the arm/hand after 4 month
Secondary Bipedal rising from sitting to standing Measure the strength at baseline
Secondary One-legged jump measure strength and balance at baseline
Secondary Standing on one leg with eyes open and standing on one leg with eyes closed Measure the balance at baseline
Secondary Jamar Measure the handstrength at baseline
Secondary PinchGauge Measure the fingers strength at baseline
Secondary EQ5D Measure self-percieved health at baseline
Secondary Bipedal rising from sitting to standing measure the strength after 4 month
Secondary One-legged jump measure strength and balance after 4 month
Secondary Standing on one leg with eyes open and standing on one leg with eyes closed measure the balance after 4 month
Secondary Jamar Measure the handstrength after 4 month
Secondary PinchGauge Measure the fingers strength after 4 month
Secondary EQ5D Measure self-percieved health after 4 month
See also
  Status Clinical Trial Phase
Completed NCT04657926 - A Trial of APPA in the Treatment of Knee Osteoarthritis Phase 2
Completed NCT02536833 - A Study Evaluating the Safety, Tolerability, and Efficacy of SM04690 Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects Phase 2
Completed NCT03014037 - Comparing Mesenchymal Stem Cell Counts in Unilateral vs. Bilateral Posterior Superior Iliac Spine Bone Marrow Aspiration N/A
Recruiting NCT05937542 - A Qualitative Investigation of CLEAT Participants
Completed NCT03644615 - A Mindfulness Program (MBSR) in the Management of Symptomatic Hip and Knee Osteoarthritis N/A
Recruiting NCT06061367 - Muscles Strength and Gait Parameteres After TKA
Withdrawn NCT04976972 - A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional Instrumentation N/A
Completed NCT05496205 - A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers Phase 1
Completed NCT03850665 - Comparison of Functional Outcome in Patients After Hip Arthroplasty Depending on Surgical Approach N/A
Completed NCT02826902 - Effect of Anesthesia on Quality of Recovery in Patients Undergoing Correctional Tibial Osteotomy - A Randomized Controlled Trial N/A
Completed NCT04402502 - Dynamic 4DCT to Examine Wrist Carpal Mechanics N/A
Completed NCT02923700 - Leukocyte-rich PRP vs Leukocyte-poor PRP for the Treatment of Knee Cartilage Degeneration: a Randomized Controlled Trial Phase 4
Completed NCT04564053 - Study of Safety, Tolerability and Pharmacokinetics of LNA043 in Japanese Osteoarthritis Participants Phase 1
Completed NCT05070871 - A Clinical Trial Investigating the Effect of Salmon Bone Meal on Osteoarthritis Among Men and Women N/A
Not yet recruiting NCT05036174 - Diphenhydramine Ointment for Knee Osteoarthritis N/A
Recruiting NCT02666443 - Low Dose Dexamethasone in Supraclavicular Blocks N/A
Recruiting NCT02912429 - Onlay vs. Inlay Patellofemoral Arthroplasty N/A
Active, not recruiting NCT02723929 - Effects of tDCS and tUS on Pain Perception in OA of the Knee
Withdrawn NCT02921594 - Kinematic Comparison of Vanguard XP and Vanguard CR Total Knee Arthroplasties N/A
Terminated NCT02820766 - Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting N/A