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- Ensaio Clínico NCT02835326
Collaborative Lifestyle Intervention Program in Knee Osteoarthritis Patients (CLIP-OA)
The Collaborative Lifestyle Intervention Program in Knee Osteoarthritis Patients: CLIP-OA
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
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Ohio
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Columbus, Ohio, Estados Unidos, 43210
- The Ohio State University
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Cuidados de suporte
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Experimental: 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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Comparador Ativo: 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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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
---|---|---|
Mobility Disability
Prazo: 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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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
---|---|---|
Anthropometric Battery
Prazo: 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
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Brian Focht, PhD, Ohio State University
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 2015H0394
- R01AG050725 (Concessão/Contrato do NIH dos EUA)
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