Project Arthritis Recovering Quality of Life Through Education 70+ (PARQVE)
Primary Purpose
Knee Osteoarthritis
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Multiprofessional treatment and Educational Program Associated (EPA+C+BCAA) with supplementation of creatine and BCAA.
Multiprofessional treatment and Educational Program Associated (EPA+C) with supplementation of creatine only.
Sponsored by

About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Osteoarthritis, Knee, Quality of Life, Sarcopenia
Eligibility Criteria
Inclusion Criteria:
- Men and women diagnosed with OAJ with or without metabolic syndrome (ie at least two of: overweight / obese, hyperglycemia, dyslipidemia, hypertension)
- Age greater than or equal to 70 years.
- Classified as degrees I to III of Kelgreen and Lawrence (K-L), that is, any degree of gonarthritis without obliteration of joint space.
- Indication of clinical treatment of OA
- Patients without disabsorbing syndrome or inflammatory diseases of the gastrointestinal tract (GIT).
- Patients not undergoing gastroplasty or surgery that altered the transit of food in the TGI (Roux "Y", for example).
- Patients with creatinine clearance greater than 60 ml / min / 1.73m2
- Patients not submitted to previous arthroplasty in the lower limbs.
- Patients not submitted to infiltration in the knees up to 6 months before the study.
- Patients with no personal history of cognitive, psychiatric and / or neurological disorders, whose symptoms presented at the time of evaluation are related or significantly interfere with the functions of attention, memory, logical reasoning, comprehension, in order to impair the assimilation of the given guidelines.
- Ability to read, understand and respond to the questionnaires
Exclusion Criteria:
- Missing the schedules and not performing the tasks as performed by the professionals.
- Patients who develop allergy or intolerance to creatine, dextrose or BCAA during the study.
Sites / Locations
- Instituto de Ortopedia e Traumatologia do Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Experimental
Control group
Arm Description
Multiprofessional treatment and Educational Program Associated (EPA+C+BCAA) with supplementation of creatine and BCAA.
Multiprofessional treatment and Educational Program Associated (EPA+C) with supplementation of creatine only.
Outcomes
Primary Outcome Measures
Participants who improve function by performing the sit to stand 30 seconds test (STS30)
Compare supplementation with creatine and BCAA to supplementation with creatine only improves the functional results of patients in the sit to stand 30 seconds (STS30)
Secondary Outcome Measures
Change of results in the sit to stand 30 seconds test
Perform sit to stand 30 seconds test, recording the number of stands a person can complete in 30 seconds, more fast better.
Change of results in the Time up and go test
Perform time up and go test, The time that a person takes to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down, faster perform better.
Change of results in the Womac questionnaire
Answer Womac Questionnaire - Ranges: minimum 0 (Better, no pain and limitation) / maximum 96 (Worst pain and limitation)
Change of results in the Lequesne questionnaire
Answer Lequesne Questionnaire - Ranges: minimum 0 (Better, no limitation) / maximum 24 (Worst limitation)
Change of results in the Visual Analogue Scale
Answer Visual Analogue Scale - Ranges: minimum 0 (Better, no pain) / maximum 100 (Worst pain)
Change of results in the EuroQol Scale
Answer EuroQol Scale - Ranges: minimum 0 (Better) / maximum 2 (Worst)
Change fat percentage
Calculate fat percentage
Change lean mass percentage
Calculate lean mass
Full Information
NCT ID
NCT04058002
First Posted
June 26, 2019
Last Updated
August 14, 2019
Sponsor
University of Sao Paulo General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04058002
Brief Title
Project Arthritis Recovering Quality of Life Through Education 70+
Acronym
PARQVE
Official Title
Project Arthritis Recovering Quality of Life Through Education 70+
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 15, 2019 (Anticipated)
Primary Completion Date
February 15, 2020 (Anticipated)
Study Completion Date
October 15, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo General Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Introduction: Quadriceps weakness was previously associated with functional impairment of osteoarthritis (OA). Evidence also suggests that muscle strength may prevent the progression of existing OA. It is estimated that the decline in muscle mass between 40 and 80 years is between 30% and 50%, with reported losses in functional capacity reaching 3% each year beyond the age of 60 years. Therefore, procedures capable of increasing the effects of exercise on muscle strength and function may be beneficial for elderly patients with knee OA. The results of our studies have shown that with each year of life the patient loses strength gain capacity. Objective: To evaluate if a multiprofessional educational program associated with BCAA and creatine supplementation improves the quality of life, function, pain and body composition of patients with OA and age greater than or equal to 70 years. METHODS: 34 patients with knee OA and age greater than or equal to 70 years will undergo an educational and physical training program lasting 20 weeks. Half of the patients will receive creatine (control) and the others will receive creatine and BCAA (study). Patients will be evaluated through functional tests (sit-up and 30-second tests and time up and go), standardized questionnaires (WOMAC and Lequesne), quality of life scales (Euroqol-EQ-5D-5L), pain (through VAS), body composition and bone density (through densitometry), and level of physical activity. All of the above parameters will be assessed at the beginning of the study and 6 and 12 months later. All project costs will be reported and a cost-effectiveness and cost-utility analysis will be performed. All project costs will be reported and a cost-effectiveness and cost-utility analysis will be performed.
Detailed Description
Osteoarthritis (OA) is the most common form of arthritis, affecting mainly women. Patients with OA present pain that usually worsens with weight support and improves with rest, as well as morning stiffness and after periods of inactivity.
Quadriceps weakness was previously associated with functional impairment of OA. Evidence also suggests that muscle strength may prevent the progression of existing OA. In fact, positive associations were found between increased quadriceps strength and self-efficacy of ambulation, reduction of pain and improvement of function, emphasizing the role of muscle strengthening in the treatment of knee OA.
It is estimated that the decline in muscle mass between 40 and 80 years is between 30% and 50%, with reported losses in functional capacity reaching 3% each year after the age of 60 years. Therefore, procedures capable of enhancing the effects of exercise on muscle strength and function may be beneficial for elderly patients with knee OA.
The results of our previous studies have shown that with each year of life the patient loses strength gain capacity.
Creatine is a natural amine endogenously synthesized by the liver, kidney and pancreas or obtained in the diet from red meat, seafood and dairy products. Creatine plays an important role in rapid energy supply, being stored mainly in the skeletal muscles (90%) as phosphocreatine, a high energy phosphate involved in the rapid resynthesis of adenosine triphosphate during muscle contraction. It has already been demonstrated that the combination of resistance training and creatine supplementation is superior to exercise alone in the elderly and has proved to be a useful tool in the elderly with knee OA.
Studies have demonstrated the need for a higher protein intake in the elderly with some studies showing greater protein synthesis and improved body composition parameters.
The investigators believe that an education and physical activity program, used in the previous work of the authors that presented improvement of WOMAC, that can be reproduced in any basic health care unit, along with supplementation with creatine and branched chain amino acids can lead to an improvement functional evaluation of elderly patients with knee OA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Osteoarthritis, Knee, Quality of Life, Sarcopenia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental
Arm Type
Experimental
Arm Description
Multiprofessional treatment and Educational Program Associated (EPA+C+BCAA) with supplementation of creatine and BCAA.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Multiprofessional treatment and Educational Program Associated (EPA+C) with supplementation of creatine only.
Intervention Type
Other
Intervention Name(s)
Multiprofessional treatment and Educational Program Associated (EPA+C+BCAA) with supplementation of creatine and BCAA.
Intervention Description
17 patients will participate in two days of lectures two-months apart on the subject of knee OA, but will also come to the hospital at months 1, 3 and 5 after the first class to consult about nutritional habits to be improved; at months 4 and 6 to participate in a group therapy session with the psychologists, 7 sessions with the physical therapy team followed by 7 sessions with the physical educators team (once a week/4 weeks and once every two weeks, three times). Patients will be supplemented with creatine 5 grams and maltodextrin 100g, 30 minutes before training. At breakfast they will also ingest 5 grams of BCAA (1,200 milligrams of leucine, 600 milligrams of isoleucine and 600 milligrams of valine per dose)
Intervention Type
Other
Intervention Name(s)
Multiprofessional treatment and Educational Program Associated (EPA+C) with supplementation of creatine only.
Intervention Description
17 patients will participate in two days of lectures two-months apart on the subject of knee OA, but will also come to the hospital at months 1, 3 and 5 after the first class to consult about nutritional habits to be improved; at months 4 and 6 to participate in a group therapy session with the psychologists, 7 sessions with the physical therapy team followed by 7 sessions with the physical educators team (once a week/4 weeks and once every two weeks, three times). Patients will be supplemented with creatine 5 grams and maltodextrin 100g, 30 minutes before training. At breakfast they will also ingest 5 grams of placebo.
Primary Outcome Measure Information:
Title
Participants who improve function by performing the sit to stand 30 seconds test (STS30)
Description
Compare supplementation with creatine and BCAA to supplementation with creatine only improves the functional results of patients in the sit to stand 30 seconds (STS30)
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change of results in the sit to stand 30 seconds test
Description
Perform sit to stand 30 seconds test, recording the number of stands a person can complete in 30 seconds, more fast better.
Time Frame
12 months
Title
Change of results in the Time up and go test
Description
Perform time up and go test, The time that a person takes to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down, faster perform better.
Time Frame
6 months and 12 months
Title
Change of results in the Womac questionnaire
Description
Answer Womac Questionnaire - Ranges: minimum 0 (Better, no pain and limitation) / maximum 96 (Worst pain and limitation)
Time Frame
6 months and 12 months
Title
Change of results in the Lequesne questionnaire
Description
Answer Lequesne Questionnaire - Ranges: minimum 0 (Better, no limitation) / maximum 24 (Worst limitation)
Time Frame
6 months and 12 months
Title
Change of results in the Visual Analogue Scale
Description
Answer Visual Analogue Scale - Ranges: minimum 0 (Better, no pain) / maximum 100 (Worst pain)
Time Frame
6 months and 12 months
Title
Change of results in the EuroQol Scale
Description
Answer EuroQol Scale - Ranges: minimum 0 (Better) / maximum 2 (Worst)
Time Frame
6 months and 12 months
Title
Change fat percentage
Description
Calculate fat percentage
Time Frame
6 months and 12 months
Title
Change lean mass percentage
Description
Calculate lean mass
Time Frame
6 months and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women diagnosed with OAJ with or without metabolic syndrome (ie at least two of: overweight / obese, hyperglycemia, dyslipidemia, hypertension)
Age greater than or equal to 70 years.
Classified as degrees I to III of Kelgreen and Lawrence (K-L), that is, any degree of gonarthritis without obliteration of joint space.
Indication of clinical treatment of OA
Patients without disabsorbing syndrome or inflammatory diseases of the gastrointestinal tract (GIT).
Patients not undergoing gastroplasty or surgery that altered the transit of food in the TGI (Roux "Y", for example).
Patients with creatinine clearance greater than 60 ml / min / 1.73m2
Patients not submitted to previous arthroplasty in the lower limbs.
Patients not submitted to infiltration in the knees up to 6 months before the study.
Patients with no personal history of cognitive, psychiatric and / or neurological disorders, whose symptoms presented at the time of evaluation are related or significantly interfere with the functions of attention, memory, logical reasoning, comprehension, in order to impair the assimilation of the given guidelines.
Ability to read, understand and respond to the questionnaires
Exclusion Criteria:
Missing the schedules and not performing the tasks as performed by the professionals.
Patients who develop allergy or intolerance to creatine, dextrose or BCAA during the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Livia Abreu
Phone
1126612473
Email
murmedicina@outlook.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guilherme P Ocampos, MD
Organizational Affiliation
University of São Paulo General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto de Ortopedia e Traumatologia do Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo
City
São Paulo
ZIP/Postal Code
05403-010
Country
Brazil
12. IPD Sharing Statement
Plan to Share IPD
No
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