- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT02835326
Collaborative Lifestyle Intervention Program in Knee Osteoarthritis Patients (CLIP-OA)
The Collaborative Lifestyle Intervention Program in Knee Osteoarthritis Patients: CLIP-OA
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
Knee OA is a chronic, progressive, degenerative disease that affects over 20 million Americans, and is cited as the primary cause for activity restriction and physical disability in older adults. The joint damage and symptoms (i.e., pain, stiffness, and fatigue) accompanying symptomatic knee OA result in activity restriction, muscle atrophy, reduced quality of life and difficulty in performance of functional tasks.
Despite the well-established benefits of the Arthritis Foundation's (AF) exercise programs, recent evidence suggests that lifestyle interventions combining Exercise and Dietary Weight Loss (EX+DWL) results in superior improvements in key clinical outcomes in older, overweight or obese knee OA patients.
Primary Aim: To compare the effects of a novel community-based EX+DWL program to AF's Walk with Ease (WWE) EX intervention on improved mobility in knee osteoarthritis (OA) patients.
Secondary Aim: To compare the cost effectiveness and effects of the EX+DWL and WWE interventions on weight loss, pain, and quality of life.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Ohio
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Columbus, Ohio, Stany Zjednoczone, 43210
- The Ohio State University
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Diagnosed with knee OA: physician documented radiographic tibiofemoral OA of one or both knees
- Overweight or Obese: BMI >25 and <40
- Knee Pain and Risk for Mobility Disability: self-reported difficulty walking ¼ mile, climbing stairs, lifting or carrying groceries, or performing other household activities due to knee pain
- Sedentary: sedentary lifestyle defined as currently participating < 20 minutes of weekly structured moderate intensity exercise occurring in bouts >10 min
- Health Status: all participants must be free of severe heart or systemic disease that would make moderate intensity exercise participation unsafe
- Age: > 50 years of age
- Stability of Residence: does not plan to move out of the Columbus metropolitan area for the duration of the study
- Consents: willing to give an informed consent and sign a HIPPA authorization form; (9) Physician Consent: treating rheumatologist and primary care physician provide medical consent for participation
- Agreeableness: willing to accept randomization and complete all assessment and intervention procedures
Exclusion Criteria:
- Health Status: any serious medical condition that precludes safe participation in an exercise program
- Study Staff Judgment: Inability to complete the study protocol, in the opinion of the study staff, due to frailty, illness, or other reasons
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Exercise and Dietary Weight Loss
For the first 6 months, participants will meet at a community center for 3 group-based sessions and 1 individual session each month.
Sessions include a 45 minute exercise component and a 45 minute dietary weight loss component.
Exercise will consist of progressive aerobic and strength training.
The dietary component will focus on decreasing caloric intake, while being nutritionally safe.
All diets will be monitored by a Registered Dietitian.
During months 7-12, participants will meet for 1 group session and 1 individual session per month.
The final 12-24 months, bimonthly phone calls are provided to the participants to aid in retention efforts.
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The EX+DWL intervention consists of group and individual exercise sessions, as well as, nutritional and dietary counseling.
Bimonthly phone calls are made in the final year of the study to aid in maintenance of the program.
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Aktywny komparator: Walk with Ease
The Arthritis Foundation's (AF) WWE is a self-management program for symptoms of arthritis (pain, fatigue, stiffness,etc.) through exercise.
It is a 6 week program involving 3 sessions per week each lasting about 60 minutes.
The WWE sessions are comprised of walking, stretching and strengthening exercises, and health education lectures.
These group classes will be lead by an AF instructor.
Each participant will complete 2 consecutive WWE classes for a total of 12 weeks in the program.
During the final week of the program, participants will be trained and transitioin to the self-directed version of WWE for maintenance of exercise.
To aid in retention efforts, phone contacts are provided to participants on a monthly basis from 4-12 months and bi-monthly from 12 to 24 months
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The WWE 6 week program consists of health education lectures on arthritis self-management, a walking exercise portion, and at- home strength exercises.
Participants will complete two consecutive WWE programs.
Monthly and bimonthly phone calls are made to participants in months 4-12 and 12-24, respectively, to aid in maintenance of the program.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Mobility Disability
Ramy czasowe: baseline up to 2 years
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This will be assessed using the 400 meter walk test (400MWT), which is the time to complete 400m as quickly as possible (without running)
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baseline up to 2 years
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
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Anthropometric Battery
Ramy czasowe: baseline up to 2 years
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Body weight and height are used to calculate Body Mass Index (BMI).
Body composition will be assessed using DEXA scans.
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baseline up to 2 years
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Functional Battery and Limitations
Ramy czasowe: baseline up to 2 years
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Stair-climb time (SCT) is a functional performance measure that involves ascending and descending a flight of 5 stairs as quickly as possible.
Limitations will be assessed using the Pepper Assessment Tool for Disability.
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baseline up to 2 years
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Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Ramy czasowe: baseline up to two years
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Scale of 0 (none) to 4 (extreme) indicating the amount of difficulty they have experienced performing basic physical function tasks in the past 48 hours due to knee OA.
The physical function subscale consists of 17 items that will be summed to produce a physical function score.
Higher scores indicating poorer function
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baseline up to two years
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Rand Medical Outcomes Study 36-item Short Form Health Survey (SF-36)
Ramy czasowe: baseline up to two years
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Health related quality of life survey consisting of mental and physical health with subscales of physical functioning, mental health, role-physical, role-emotional, bodily pain, general health, vitality, and social functioning
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baseline up to two years
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Dietary intake
Ramy czasowe: baseline up to two years
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Dietary intake will be assessed by a registered dietician using the Daily food record measure.
One weekend and 2 weekdays will be assessed.
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baseline up to two years
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Social Cognitive Process Measures
Ramy czasowe: baseline up to two years
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Physical activity barriers self-efficacy scale, Satisfaction with function and appearance scale, Multiple exercise self-regulatory self-efficacy scale, the weight efficacy lifestyle questionnaire (WEL), goal commitment and goal difficulty, arthritis self-efficacy, and pain acceptance.
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baseline up to two years
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Change in physical activity
Ramy czasowe: baseline up to two years
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Physical activity will be assessed using the Community Healthy Activities Model Program For Seniors (CHAMPS) and Lifecorder EX Accelerometer
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baseline up to two years
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Cost effectiveness
Ramy czasowe: baseline up to two years
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The cost-effectiveness of the EX+DWL intervention compared to the WWE [program will be calculated as the ratio of additional cost per participant per increment of effectiveness.
Effectiveness is based on improvement in the 400 MWT and the Quality of Well-being Scale- Self Administered (to calculate the Quality Adjusted Life Years).
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baseline up to two years
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Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Brian Focht, PhD, Ohio State University
Publikacje i pomocne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 2015H0394
- R01AG050725 (Grant/umowa NIH USA)
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na Exercise and Dietary Weight Loss
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University of California, San FranciscoNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Zakończony
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Walter Reed Army Medical CenterZakończony
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The Miriam HospitalNational Institute on Minority Health and Health Disparities (NIMHD)Jeszcze nie rekrutacja