Enhancing the Effectiveness of Physical Therapy for People With Knee Osteoarthritis
22 июня 2015 г. обновлено: g. kelly fitzgerald, Agency for Healthcare Research and Quality (AHRQ)
Enhancing the Effectiveness of Physical Therapy for People With Knee
The overall aim of the project is to examine the clinical and cost-effectiveness of utilizing booster sessions(periodic face-to-face follow-up appointments that take place several weeks or months following discharge from the supervised therapy program designed to review the patient's current rehabilitation program, troubleshoot any problems with the program, and make recommendations for program progression or modification) in the delivery of exercise therapy, and supplementing exercise therapy with manual therapy techniques(manually applied treatment techniques such as joint mobilization/manipulation, manual traction, soft tissue manipulations, passive stretching and range of motion).
The investigators will do this in a randomized, multi-center, clinical trial.
The investigators hypothesize that adding manual therapy techniques will be more clinically effective than exercise alone and that using booster sessions will maintain longer term clinical effects and be more cost-effective than not using booster sessions.
Обзор исследования
Статус
Завершенный
Условия
Вмешательство/лечение
Подробное описание
Exercise therapy (ET) is effective as the first line of treatment for reducing pain and disability in patients with knee osteoarthritis (OA), but studies show its effects diminish considerably over time.
'Booster' intervention sessions (periodic face-to-face follow-up appointments following discharge from supervised therapy designed to review and progress the patient's home program, troubleshoot problems with the program, etc.) have been recommended to make beneficial effects endure however this recommendation has not been adequately tested.
There are also indications that manual therapy (MT), manually applied treatment techniques such as joint mobilization/manipulation, manual traction, soft tissue manipulations, and passive stretching, when combined with ET, may improve the overall effectiveness of rehabilitation for reducing pain and disability, and, may significantly delay or reduce the need for total knee arthroplastic surgery and reduce medication intake in people with knee OA.
However, current published evidence-based treatment guidelines indicate there is not enough data to make a definitive recommendation regarding the use of MT with ET in rehabilitation programs.
Therefore, the overall aim of the project is to examine the clinical and cost-effectiveness of utilizing booster sessions in the delivery of ET, and supplementing ET with MT techniques.The study will be a multi-center,randomized clinical trial, using a 2 x 2 factorial design (factor 1 = booster vs no booster, factor 2 = ET alone vs ET + MT).
Three hundred subjects (100 per study site) with knee OA will be randomized to one of the following groups: 1) ET - no booster, 2) ET - with booster, 3) MT + ET - no booster sessions, 4) MT + ET - with booster sessions.
Clinical outcome measures (WOMAC, knee pain, global rating of change and performance-based measures of function) will be taken at baseline (prior to randomization), at the completion of the initial therapy sessions (9 weeks) and at 1 year follow-up.
The primary endpoint for clinical outcome will be the WOMAC at 1 year.For the cost effectiveness analysis, the primary cost outcome will be osteoarthritis treatment costs from the societal perspective, which will include health system costs for implementing each intervention, medical/surgical costs (primary, secondary, and tertiary care costs), and personal costs to participants (travel, non-funded medications, time off work, and quality-of-life burdens).
The primary effectiveness outcome measure will be quality-adjusted life-years (QALYs), derived using quality of life utilities from EQ-5D scores.
Cost and effectiveness values between interventions will be compared via incremental cost-effectiveness ratios, yielding incremental costs per QALY gained when a given intervention is chosen.
Secondary analyses will examine cost-effectiveness from health system and from patient perspectives.
Cost and effectiveness data will be obtained at 1 year and 2 year follow-ups.
The 2 year follow-up will be the primary endpoint for the cost-effectiveness analysis.
Тип исследования
Интервенционный
Регистрация (Действительный)
300
Фаза
- Фаза 2
- Фаза 3
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, Соединенные Штаты, 15260
- University of Pittsburgh
-
-
Texas
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San Antonio, Texas, Соединенные Штаты
- Army-Baylor University
-
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Utah
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Salt Lake City, Utah, Соединенные Штаты
- Intermountain Healthcare
-
-
Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
40 лет и старше (Взрослый, Пожилой взрослый)
Принимает здоровых добровольцев
Нет
Полы, имеющие право на обучение
Все
Описание
Inclusion Criteria:
- 40 years of age or older
- Meet the American College of Rheumatology (ACR) clinical criteria for a diagnosis of knee OA. The ACR clinical criteria for knee OA includes knee pain plus 3 of the following 6 criteria:
- age > 50 years,
- morning stiffness of < 30 minutes,
- crepitus on active movement,
- tenderness of the bony margins of the joint,
- bony enlargement of the joint noted on exam,
- lack of palpable warmth of the synovium. Based on this criteria, a subject who is less than 50 years but has knee pain and 3 of the other 5 criteria would also be classified as having knee OA.
Exclusion Criteria:
- do not meet the ACR clinical criteria for knee OA,
- are scheduled for total knee arthroplasty (TKA) surgery,
- have undergone TJA surgery on any lower extremity joint,
- exhibit uncontrolled hypertension (i.e. individuals not currently taking medication for hypertension whose systolic blood pressure is greater than 140 mm Hg or diastolic blood pressure greater than 90 mm Hg at rest),
- have complaints of low back pain or other lower extremity joint pain that affects function at the time of recruitment,
- have a history of neurological disorders that would affect lower extremity function (stroke, peripheral neuropathy, parkinson's disease, multiple sclerosis, etc.),
- are women who are pregnant.
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Факторное присвоение
- Маскировка: Двойной
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Активный компаратор: exercise
Subjects in this arm receive 12 exercise sessions in 9 weeks.
|
The program starts with a 10 minute aerobic exercise warm-up (treadmill walking or stationary cycling).
Subjects then perform a series of strengthening, stretching, and neuromuscular control activities which are core exercises for the program and mandatory.
In addition to the above core exercises, therapists have the option to select additional optional exercise activities, based on the initial examination findings.
These exercises will address strength or flexibility in the hip, and ankle if impairments are identified in the initial examination.
|
|
Активный компаратор: exercise + manual therapy
Subjects in this group receive exercise combined with manual therapy techniques for 12 sessions in 9 weeks.
|
The program starts with a 10 minute aerobic exercise warm-up (treadmill walking or stationary cycling).
Subjects then perform a series of strengthening, stretching, and neuromuscular control activities which are core exercises for the program and mandatory.
In addition to the above core exercises, therapists have the option to select additional optional exercise activities, based on the initial examination findings.
These exercises will address strength or flexibility in the hip, and ankle if impairments are identified in the initial examination.
The manual therapy (MT)techniques are maneuvers that are applied with manual force from the treating therapist.
The MT techniques will include a series of accessory motion techniques, manual stretching , and soft tissue manipulation (deep massage to muscles and connective tissues associated with knee function).
Core techniques include anterior-posterior and posterior-anterior tibiofemoral translations, superior-inferior and medial-lateral patellofemoral mobilizations, knee flexion and extension mobilizations that may be combined with varus-valgus stresses,medial-lateral tibial rotations, manual stretching of the quadriceps, rectus femoris, hamstring, and gastrocnemius muscles, and soft tissue manipulations of the quadriceps, peri-patellar tissues, hamstring, hip adductors, and gastroc-soleus muscle groups.
There are optional MT techniques for the hip, and foot and ankle joints that can be selected by the therapist based on initial examination findings.
|
|
Экспериментальный: exercise + booster
subjects in this arm will receive exercise sessions delivered with booster sessions (8 sessions in the first 9 weeks, 2 sessions at 5 months, 1 session at 8 months, and 1 session at 11 months).
|
The program starts with a 10 minute aerobic exercise warm-up (treadmill walking or stationary cycling).
Subjects then perform a series of strengthening, stretching, and neuromuscular control activities which are core exercises for the program and mandatory.
In addition to the above core exercises, therapists have the option to select additional optional exercise activities, based on the initial examination findings.
These exercises will address strength or flexibility in the hip, and ankle if impairments are identified in the initial examination.
|
|
Экспериментальный: exercise + manual therapy + booster
Subjects in this arm will receive exercise combined with manual therapy techniques and booster sessions.
|
The program starts with a 10 minute aerobic exercise warm-up (treadmill walking or stationary cycling).
Subjects then perform a series of strengthening, stretching, and neuromuscular control activities which are core exercises for the program and mandatory.
In addition to the above core exercises, therapists have the option to select additional optional exercise activities, based on the initial examination findings.
These exercises will address strength or flexibility in the hip, and ankle if impairments are identified in the initial examination.
The manual therapy (MT)techniques are maneuvers that are applied with manual force from the treating therapist.
The MT techniques will include a series of accessory motion techniques, manual stretching , and soft tissue manipulation (deep massage to muscles and connective tissues associated with knee function).
Core techniques include anterior-posterior and posterior-anterior tibiofemoral translations, superior-inferior and medial-lateral patellofemoral mobilizations, knee flexion and extension mobilizations that may be combined with varus-valgus stresses,medial-lateral tibial rotations, manual stretching of the quadriceps, rectus femoris, hamstring, and gastrocnemius muscles, and soft tissue manipulations of the quadriceps, peri-patellar tissues, hamstring, hip adductors, and gastroc-soleus muscle groups.
There are optional MT techniques for the hip, and foot and ankle joints that can be selected by the therapist based on initial examination findings.
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change in Western Ontario and McMaster University Osteoarthritis Index (WOMAC)
Временное ограничение: Change from baseline at 9 weeks, 1 year and 2 years
|
Self report measure of pain, stiffness, and physical function for people with knee osteoarthritis.
|
Change from baseline at 9 weeks, 1 year and 2 years
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Cost/Utility Ratio
Временное ограничение: 2 years
|
In the analysis, the effectiveness term will be quality adjusted life years, which is the product of the quality of life utility associated with a health state and the length of time lived in that state, summed over time.
Utilities are a measure of preference for a health state and range from 0 (death) to 1 (perfect health).
In this analysis, utilities will be derived from EQ-5D scores.
The cost-effectiveness ratio (or, in this analysis, the cost-utility ratio) is the difference in cost divided by the difference in quality-adjusted life-years between intervention groups.
|
2 years
|
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Change in Numeric Knee Pain Rating Scale
Временное ограничение: Change from Baseline to 9 weeks, 1 and 2 years
|
Subjects will rate their worst knee pain in the last 24 hours using an 11 point numeric pain rating scale with 0 representing "no pain" and 10 representing " the worst pain imaginable."
|
Change from Baseline to 9 weeks, 1 and 2 years
|
|
Global Rating of Change
Временное ограничение: Change from baseline to 9 weeks, 1 and 2 years
|
The global rating of change is a 15 item scale in which subjects will rate the degree to which their knee condition has changed from the time treatment was initiated to the present.24
The subject responds to the following query: "Please rate your overall knee's condition from the time you began treatment until now (check only one)."
The items range from "A very great deal better" to "A very great deal worse."
|
Change from baseline to 9 weeks, 1 and 2 years
|
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Change in Timed Up and Go Test Time
Временное ограничение: Change from Baseline to 9 weeks and 1 year
|
On the command "go" subjects will stand up from a chair, walk 3 meters, turn around, return to the chair and sit down.
The time it takes to complete this task will be recorded.
|
Change from Baseline to 9 weeks and 1 year
|
|
Change in 30 second time chair rise test.
Временное ограничение: Change from Baseline to , 9 weeks, 1 year
|
Subjects will be seated with their arms crossed in front of their chest.
On the command "go" subjects will stand up and sit down for as many trials as they can in a 30 second period.
|
Change from Baseline to , 9 weeks, 1 year
|
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Change in Self-paced Walk Test Time
Временное ограничение: Change from Baseline to 9 weeks, 1 year
|
Subjects will walk 4 lengths of a 10 meter indoor course in response to the instructions, "Walk as quickly as you can without overexerting yourself."
|
Change from Baseline to 9 weeks, 1 year
|
|
Change in Pain belief screening instrument
Временное ограничение: Change in Baseline to 1 year
|
7 item instrument that queries the subject about their pain and how they believe pain limits or does not limit their ability to perform daily activities, social and liesure interactions, mood, etc.
|
Change in Baseline to 1 year
|
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Change in Beck Anxiety Index (BAI)
Временное ограничение: Change from Baseline to 1 year
|
The BAI consists of 21 items, each item scored 0-3, with higher scores representing higher levels of anxiety.
|
Change from Baseline to 1 year
|
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Change in Center for Epidemiological Studies Depression Scale (CES-D)
Временное ограничение: Change from Baseline to 1year
|
The CES-D is a 20-item self-report depression scale, each item scored 0-3, with higher scores representing greater symptoms of depression.
|
Change from Baseline to 1year
|
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Change in EQ-5D
Временное ограничение: Change from Baseline to 1 and 2 years
|
The EQ-5D is a generic health-related quality of life measure.
The EQ-5D consists of the following five dimensions: 1) Mobility, 2) Self-care, 3) Usual activities, 4) Pain/discomfort, and 5) Anxiety/depression (AD).Each dimension has three possible levels (i.e., 1, 2, or 3), representing "no problems," "some problems," and "extreme problems," respectively.
Respondents are asked to choose one level that reflects their "own health state today" for each of the five dimensions.
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Change from Baseline to 1 and 2 years
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OARSI Responder Criteria
Временное ограничение: 9 weeks and 1 year
|
Responder criteria included 1) greater than or equal to 50% improvement in WOMAC pain or WOMAC function and an absolute improvement of greater than or equal to 20, or 2) improvement in at least 2 of the following 3 scores: 20% improvement in pain and absolute change ≥ 10 on WOMAC pain score, 20% improvement in pain and absolute change ≥ 10 on WOMAC function score, or moderate or greater improvement (≤ 4) on a 15 point global rating of change scale.
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9 weeks and 1 year
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Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Следователи
- Главный следователь: G. Kelley Fitzgerald, PT, PhD, University of Pittsburgh
- Главный следователь: Julie M Fritz, PT, PhD, Intermountain Healthcare, Salt Lake City, UT
- Главный следователь: John D Childs, PT, PhD, Army-Baylor University, San Antonio, TX
- Главный следователь: J. Haxby Abbott, PT, PhD, University of Otago, Dunedin, New Zealand
Публикации и полезные ссылки
Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.
Общие публикации
- Bove AM, Smith KJ, Bise CG, Fritz JM, Childs JD, Brennan GP, Abbott JH, Fitzgerald GK. Exercise, Manual Therapy, and Booster Sessions in Knee Osteoarthritis: Cost-Effectiveness Analysis From a Multicenter Randomized Controlled Trial. Phys Ther. 2018 Jan 1;98(1):16-27. doi: 10.1093/ptj/pzx104.
- Fitzgerald GK, Fritz JM, Childs JD, Brennan GP, Talisa V, Gil AB, Neilson BD, Abbott JH. Exercise, manual therapy, and use of booster sessions in physical therapy for knee osteoarthritis: a multi-center, factorial randomized clinical trial. Osteoarthritis Cartilage. 2016 Aug;24(8):1340-9. doi: 10.1016/j.joca.2016.03.001. Epub 2016 Mar 10.
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования
1 апреля 2011 г.
Первичное завершение (Действительный)
1 апреля 2015 г.
Завершение исследования (Действительный)
1 апреля 2015 г.
Даты регистрации исследования
Первый отправленный
23 февраля 2011 г.
Впервые представлено, что соответствует критериям контроля качества
11 марта 2011 г.
Первый опубликованный (Оценивать)
14 марта 2011 г.
Обновления учебных записей
Последнее опубликованное обновление (Оценивать)
23 июня 2015 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
22 июня 2015 г.
Последняя проверка
1 июня 2015 г.
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- 1R01HS019624-01 (Грант/контракт AHRQ США)
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .