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P.A.R.Q.V.E III - Comparison of the Educational Program With and Without Multidisciplinary Care

PARQVE - Project Arthritis Recovering Quality of Life by Means of Education - A Prospective Randomized Study Comparing the Educational Program With and Without Multidisciplinary Care

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02917655
Acronym
PARQVE3
Enrollment
90
Registered
2016-09-28
Start date
2016-11-01
Completion date
2021-07-15
Last updated
2019-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Metabolic Diseases

Keywords

Education, Quality of Life, Osteoarthritis, Metabolic Syndrome

Brief summary

BACKGROUND: Osteoarthritis (OA), and particularly knee osteoarthritis (KOA) is a disorder that greatly impairs the quality of life of patients and its incidence increases with longevity, obesity and lower socioeconomic and educational level. It is expected that 40% of people over 60 have symptomatic OA of the knees and hips. The core treatment of OA is education, weight loss and increased physical activity. We create an educational program that improved function of the patients given by the sit-to-stand 30 seconds test (STS30). However, weight loss, an important foundation of clinical treatment, was only effective (more than 2 points in BMI) in 10% of the program participants. For greater effectiveness in weight loss and adherence to physical activity, we prepared an intensive program with more intensive nutritional care, psychological, physical therapy and physical trainers and compare the existing program educators. OBJECTIVE: To compare an educational program isolated to an educational program associated with nutritional consultations, group therapy sessions and progressed physiotherapy sessions to sessions with physical educators in patients with KOA and comorbidities (metabolic syndrome). METHODS: Ninety patients with OAJ and co-morbidities (Two or more of: overweight or obesity, hyperglycemia, dyslipidemia, hyperuricemia, high blood pressure) will be divided into two groups: study (S) and control (C). Both groups will attend the two-day multi-professional classes on OA with two months interval. But the study group will also make three group consultations about nutrition, 1 extra session of group therapy with psychology team and 7 exercise sessions in groups with physical therapy and subsequently 7 sessions with physical educators. The groups will be evaluated for weight, height (to calculate BMI), waist-hip ratio, percentage of body fat, consumption of daily medications, WOMAC, Lequesne, IPAQ, Tampa Scale for Kinesiophobia (TSK), Sit to stand 30 seconds test (STS30), timed-up- and-go (TUG) and six minute test. At inclusion, six, twelve and 24 months after the classes.

Detailed description

Given the inclusion criteria, patients undergo pre-evaluation by the multidisciplinary group composed of teams of orthopedic doctors, nutritionists, physical therapists, physical educators: Orthopedics - it is treating the patients according to the guidelines of OARSI, offering everything we have for the treatment of OA at the Hospital das Clinicas. Nutrition - It will measure the skinfold of all patients at baseline and at six and twelve months. As the draw, will attend the study group at 1, 3 and 5 months after the first class and the control group lose weight significantly less than the study group will meet the control group after one year in the same manner than has undergone the study group . Physiotherapy - Undertake the test and sit ups, Timed-Up-and-Go (TUG) test and Sit to stand 30 seconds test (STS30) including six, twelve and 24 months after inclusion. The physiotherapy group will care study group sessions in a group of patients once a week for 4 weeks, 2 times a week for 1 month and 1x / month in the third month, giving exercises to be performed daily and charging them through the registration of patients. If the results of six and twelve months show better in the study group, the control group will do the same interventions the study group one year later. Physical Education - will apply the questionnaire International Physical Activity Questionnaire, IPAQ, Tampa Scale for Kinesiophobia (TSK) and will make up test and down stairs and evaluating short version flexibility, inclusion, six, 12 and 24 months. After three months of exercise guided by physiotherapists, the study group will begin an exercise program with physical education teachers to become able to carry out alone or join a gym at the end of the sixth month of the program. It will also provide weekly classes for 1 month, biweekly in the second month and last month in the third charging the daily activities in the record of the patient's notebook.

Interventions

BEHAVIORALWomac

Answer WOMAC at baseline, 6, 12 and 24 months.

BEHAVIORALLequesne

Answer Lequesne at baseline, 6, 12 and 24 months.

BEHAVIORALNumerical Rating Scales (NRS)

Answer NRS at baseline, 6, 12 and 24 months.

BEHAVIORALIPAQ

Answer IPAQ at baseline, 6, 12 and 24 months.

BEHAVIORALSTS30

Perform the STS30 at baseline, 6, 12 and 24 months.

BEHAVIORALTUG

Perform the TUG at baseline, 6, 12 and 24 months.

BEHAVIORALSix-minute Test

Perform the six-minute test at baseline, 6, 12 and 24 months.

BEHAVIORALTwo days of lectures

Participate in two days of classes about KOA, with the seven teams (orthopedics, psychology, physical therapy and fitness, occupational therapy, social workers and nutritionist).

BEHAVIORALSession with the psychologists

Participate in a extra session group with the psychology team about their experiences with the program

BEHAVIORALSessions with the physical therapy team

Participate in a extra session group with the physical therapists

BEHAVIORALSessions with the physical educators team

Participate in a extra session group with the physical educators

BEHAVIORALNutritional habits to be improved

Attend 3 extra meetings about nutrition.

BEHAVIORALTampa Scale for Kinesiophobia (TSK)

Answer Tampa Scale for Kinesiophobia (TSK) at baseline, 6 months, 12 and 24 months.

Sponsors

University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Men and women diagnosed with KOA with comorbidities (metabolic syndrome, ie, Osteoarthritis Knee + at least two of: overweight / obesity, hyperglycemia, dyslipidemia, hyperurecemia, hypertension, polyarthrosis) and up to 75 years old, capable of reading, understand and responding to the WOMAC questionnaire. * Classified as stages I to III Kelgreen and Lawrence (K-L), i.e. without any degree of gonarthritis obliteration of joint space narrowing. * With clinical treatment indication of OA.

Exclusion criteria

* Patients who have cognitive, and psychiatric or neurological disorders, whose symptoms during the evaluation are related to or significantly interfere in the functions of attention, memory, logical reasoning, understanding, interaction with the group, that would prevent assimilation of the given guidelines. * Missing interventions

Design outcomes

Primary

MeasureTime frameDescription
Evaluate function with the TUG (Time-up-Go test)Baseline, 6, 12 and 24 monthsApply TUG (Time-up-Go test) The data will be evaluated with absolute measures and changes in respect to baseline values at 6, 12 and 24 months.

Secondary

MeasureTime frameDescription
Evaluate improvement in functionBaseline, 6, 12 and 24 monthsApply the Lequesne questionnaire
Evaluate percentage of body fat.Baseline, 6, 12 and 24 monthsNine skinfolds measurements
Evaluate improvement in painBaseline, 6, 12 and 24 monthsApply the WOMAC questionnaire WOMAC (The Western Ontario and McMaster Universities Osteoarthritis Index)
Evaluate function with the STS30 (Sit to Stand 30 SecondsTest)Baseline, 6, 12 and 24 monthsApply STS30 (Sit to Stand 30 SecondsTest)
Evaluate the consumption of drugsbaseline to 6 monthsBoth groups, starting from inclusion will record the daily consumption of drugs (baseline to 6 months)
Level of physical activityBaseline, 6, 12 and 24 monthsApply International Questionnaire physical activity Questionnaire-IPAQ short version.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026