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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02562833
Other study ID # PLENO-FMH-1
Secondary ID
Status Completed
Phase N/A
First received September 23, 2015
Last updated April 20, 2016
Start date February 2015
Est. completion date October 2015

Study information

Verified date April 2016
Source Technical University of Lisbon
Contact n/a
Is FDA regulated No
Health authority Portugal: Ethics Committee for Clinical Research
Study type Interventional

Clinical Trial Summary

The PLE²NO (in Portuguese Education and Exercise Free Program for osteoarthritis) is a self-management and exercise program specific for elderly with knee osteoarthritis (OA), with the goals of managing OA symptoms, improving physical fitness, and developing self-efficacy and self-management of pathology.


Description:

Participants were randomly assigned to one of two groups: (1) Self-management and Exercise (2) Educational. Both groups received glucosamine and chondroitin sulfate supplement during the intervention. Blinding of participants was not possible due to the nature of the intervention; however, assessors were blinded to group allocation. The PLE2NO (in Portuguese Education and Exercise Free Program for osteoarthritis) is a community-based program with two components: self-management and exercise. Each session lasted 90 minutes, and the first 30 minutes corresponded to a self-management part and the remaining 60 minutes to the exercise program. The program was offered in a group format, encouraging peer interactions and socialization that can help counteract feelings of depression and isolation. The self-management program is based on the program developed at Stanford University, the Chronic Disease Self-Management Program which the purpose is developing self-efficacy based on social cognitive theory. The exercise program comprised both health related (strength, flexibility) and skill-related (agility, balance, speed and power) physical fitness components, and was based on Fit an Strong Program, on Exercise for People with Arthritis (FEPA) and also on the program Takin Control with Exercise (Arthritis Foundation). The program will last for 3 months and 6 months of follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date October 2015
Est. primary completion date February 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

1. Age over than or equal to 60 years;

2. Bilateral or unilateral OA of the knee diagnosed according to clinical and radiological criteria of the American College of Rheumatology (ACR)(Altman et al., 1986);

3. Independent mobility;

4. and reading and writing knowledge.

Exclusion Criteria:

1. Not be involved in another intervention program (exercise, education or physical therapy;

2. Do not use supplements (chondroitin sulfate and / or glucosamine) for at least three months;

3. Have other pathology (cardiovascular, respiratory, musculoskeletal, cancer) that prevents physical exercise;

4. Mental / psychological state hindering understanding of the program;

5. Having undergone surgery for knee replacement or going perform this surgery in the next eight months;

6. Being allergic to shellfish;

7. Have made injections of corticosteroids or hyaluronic acid in the last 6 months

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Self-Management and exercise
Self-Management and exercise It is a 3 months intervention where the participants were enrolled two times per week, 90 minutes each session, first 30 minutes were allocated for the self-management component and the remaining 60 minutes for the exercise component. Additionally,participants received glucosamine and chondroitin sulfate supplement.
Educational
This group received an educational book with information about OA features, treatment modalities and exercise education with illustration. Additionally, a monthly educational session each with one hour and a half duration, in total 3, where joint protections strategies, OA self-management and exercise contents were transmitted. Additionally,participants received glucosamine and chondroitin sulfate supplement.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Technical University of Lisbon

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline knee OA symptoms to 3 month, assessed by Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire. Change from baseline to 3 month Yes
Primary Change from baseline self-efficacy to 3 month, assessed by Self-efficacy for managing Chronic Disease - 6-Item Scale questionnaire. Change from baseline to 3 month Yes
Primary Change from baseline functional strength to 3 month, assessed by Five repetition sit to stand test. Change from baseline to 3 month Yes
Primary Change from baseline cardiorespiratory endurance to 3 month, assessed by Six Minutes' Walk test. Change from baseline to 3 month Yes
Primary Change from baseline flexibility to 3 month, assessed by Chair Sit and Reach test, and the Back Scratch test. Change from baseline to 3 month Yes
Primary Change from baseline hand grip strength to 3 month, assessed by hand grip dynamometer test. Change from baseline to 3 month Yes
Secondary Change from baseline health related quality of life to 3 month, assessed by perception of health and quality of life five dimension, five levels (EuroQol - EQ-5D-5L) questionnaire. Change from baseline to 3 month Yes
Secondary Change from baseline self-management behaviors to 3 month, Use of cognitive symptom management techniques, Communication with Physicians questionnaires. Change from baseline to 3 month Yes
Secondary Change from baseline physical activity level to 3 month, assessed by International Physical Activity Questionnaire (IPAQ). Change from baseline to 3 month Yes
Secondary Change from baseline gait speed to 3 month, assessed by Six-meters test. Change from baseline to 3 month Yes
Secondary Change from baseline balance to 3 month, assessed by Standing Balance test. Change from baseline to 3 month Yes
Secondary Change from baseline mobility to 3 month, assessed by Timed "up-and-go" test. Change from baseline to 3 month Yes
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