Osteoarthritis Clinical Trial
Official title:
Massage Therapy for Osteoarthritis of the Knee
The study is a randomized, controlled clinical trial that investigates the efficacy ogf
massage therapy for 66 patients with pain secondary to osteoarthritis of the knee. It is a
wait-list design where subjects and randomly assigned to either Group A or Group B. Group A
receives two months of massage while Group B is wait-listed, receives two months of usual
care. At the conclusion of the wait period, Group B receives two months of massage. In all
cases, subjects continue to receive conventional medical care for their OA symptoms.
Outcome measures include a WOMAC questionnaire, a visual analog pain scale, time to walk
fifty feet and range of motion of the knee (using a goniometer). A research assistant,
competent in appropriate subject assessment obtains the outcome measures. Change in
medication use is tracked by the use of patient diaries. Assessments of subjects, occurs at
baseline, and week 8 and 16 in both the intervention and control groups.
The Yale-Griffin Prevention Research Center has received funding from the Centers for
Disease Control and Prevention to conduct the Complementary and Alternative Medicine (CAM)
Outcomes Research Project (CORP). CORP includes a systematic review of the CAM literature
and the development of pilot studies assessing selected CAM interventions. The first year
efforts of the CORP research team have culminated in the selection of pilot studies
involving three public health priority conditions (attention deficit hyperactivity disorder,
asthma, and osteoarthritis) and common CAM interventions. A pilot study investigating the
effects of a massage therapy intervention for osteoarthritis is detailed in this
application.
Osteoarthritis (OA), the most common form of arthritis, is a slowly progressive degenerative
disease of joint cartilage that afflicts 30 million Americans (Praemer A, Furner S, Rice D.
Musculoskeletal Conditions in the United States, p 40: American Academy of Orthopaedic
Surgeons, 1992). It becomes more prevalent with advancing age (Peyron JG. Osteoarthritis:
The Epidemiologic ViewPoint. Clin Orthop, 213:13-19, 1986). Nearly half of America's elderly
suffer from osteoarthritis, and arthritis is the most frequently reported chronic condition
in the elderly (Praemer A, Furner S, Rice D. Musculoskeletal Conditions in the United
States, p 36: American Academy of Orthopaedic Surgeons, 1992).
Osteoarthritis affects approximately 3 out of every 100 Americans below age 45 and more than
a quarter of Americans between the ages of 45 and 64 suffer from this disabling disease
(National Center for Health Statistics. Current Estimates from the National Health Interview
Survey, 1988; Vital and Health Statistics. Series 10: No. 173, DHHS Pub. No. (PHS) 89-1501.
Public Health Service, Hyattsville, MD, Oct. 1989; Kelsey JL, Hochberg MC. Epidemiology of
Chronic Musculoskeletal Disorders. Am Rev Public Health, 91:379-401, 1988).
Osteoarthritis of the hip or knee is particularly disabling because it limits ambulation,
but the affliction also strikes the hands, the spine, and the feet with the same destructive
joint process (Felson DT. Epidemiology of Osteoarthritis: Prevalence and Risk Factors.
Osteoarthritis Disorders, American Academy of Orthopaedic Surgeons, 1995). The endpoint of
the OA disease process is total loss of joint cartilage in the affected area and the need
for joint replacement.
The high prevalence of arthritis in the population is reflected in the economic burden
engendered to treat those afflicted. The total cost of conventional treatments for arthritis
in 1988, for example, was estimated at 54.6 billion dollars (Lazenby HC, Letsch SW. National
Health Expenditures 1989; Health Care Financing Review, 12(2):1-26, 1990). Conventional
treatments for OA include pain medication (NSAIDS and cox-2 inhibitors), exercises, hot/cold
therapy, steroid injections and, eventually, surgery to repair the joint (Felson DT.
Epidemiology of Osteoarthritis: Prevalence and Risk Factors. Osteoarthritis Disorders,
American Academy of Orthopaedic Surgeons, 1995). Despite conventional treatment, OA is a
progressive disease that frequently leads to chronic pain and disability.
Massage therapy is proposed as an effective treatment for diminishing the symptoms and
improving the disease course of osteoarthritis. Massage therapy can accomplish these goals
by increasing local circulation to the affected joint, improving the tone of supportive
musculature, enhancing joint flexibility and relieving pain (J Spinal Cord Med 2001 Spring;
24(1): 54-62.).
Massage therapy has been evaluated and found to have effectiveness as an adjunct treatment
for pain secondary to cancer (Effects of massage on pain intensity: analgesics and quality
of life in patients with cancer pain: A pilot study of a randomized clinical trial conducted
within hospice care delivery. Wilkie, DJ et al.) as well as low back pain syndrome (Preyde,
M. Effectiveness of massage therapy for subacute low-back pain. Journal Burn Care & Rehab
2000; 21(3): 189-193.). It also has been shown to be beneficial for patients with chronic
pain following spinal cord injury (Nayak S, Matheis RJ, Agostinelli S, Shiflett SC. The use
of complementary and alternative therapies for chronic pain following spinal cord injury: a
pilot survey. CMAJ 2000; 162(13): 1815-1820). In a randomized, open clinical trial, a series
of classical Swedish massage therapy sessions was found to be as effective as conventional
analgesic therapy for chronic rheumatic pain. (Ernst E. Complementary and alternative
medicine for pain management in rheumatic disease. Current Opinion in Rheum 2002; 14:58-62).
However, to date, no study has specifically evaluated the effectiveness of massage therapy
for osteoarthritis.
The proposed study is a randomized, controlled clinical trial to investigate the efficacy of
massage therapy for patients with pain secondary to osteoarthritis of the knee. It is a
wait-list design where subjects will be randomly assigned to either Group A or Group B.
Group A will receive two months of massage while Group B is wait-listed, receiving two
months of usual care. At the conclusion of the wait period, Group B will receive two months
of massage. In all cases, subjects will continue to receive conventional medical care for
their OA symptoms.
Outcome measures will include a WOMAC questionnaire (see Appendix A), a visual analog pain
scale (see Appendix B), time to walk fifty feet, and range of motion of the knee (using a
goniometer). An athletic trainer, competent in appropriate subject assessment, will obtain
the outcome measures (see Appendix C for data collection form). Change in medication use
will be tracked by the use of patient diaries (see Appendix D). Assessment of subjects will
occur at baseline, and weeks 8 and 16 in both the intervention and control groups.
The intervention will consist of one-hour massage therapy sessions as follows:
Weeks one through four: twice weekly Weeks five through eight: weekly
Initial treatments are given with greater frequency to "build a loading dose" of massage
treatments, effecting a greater impact at the onset of treatment. The preponderance of
published studies built in twice-weekly massage for four to five weeks at the onset of
treatment (Field, T. et al. Bulimic adolescents benefit from massage therapy. Adolescence
1997 33, 131; Leivadi, S. et al. Massage therapy and relaxation effects on university dance
students. Journal of Dance Medicine & Science 1999, 3, 108-112).
Nationally certified and licensed massage therapists who have graduated from an accredited
school of massage therapy will give the massage therapy intervention. The therapists will
follow standard Swedish full-body therapeutic massage technique. In order to minimize
practitioner variability of treatment, a standardized protocol incorporating a sequence of
strokes (effleurage, petrissage, tapotement) has been developed (see Appendix E). Subjects
will remain supine or prone for the full hour of treatment, turning over roughly at the
halfway point.
The second group will begin receiving the identical intervention after the first group has
completed its treatment. Weekly phone calls to encourage the second group will be made to
minimize attrition. The first group will be followed via phone interviews, with follow-up
data collected until the conclusion of the study.
Subjects will be men and women with an established diagnosis of OA meeting ACR criteria, 35
years of age or greater, with a score of 4-9 on a visual analogue scale. Subjects will not
be excluded based on gender or race.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04657926 -
A Trial of APPA in the Treatment of Knee Osteoarthritis
|
Phase 2 | |
| Completed |
NCT02536833 -
A Study Evaluating the Safety, Tolerability, and Efficacy of SM04690 Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
|
Phase 2 | |
| Completed |
NCT03014037 -
Comparing Mesenchymal Stem Cell Counts in Unilateral vs. Bilateral Posterior Superior Iliac Spine Bone Marrow Aspiration
|
N/A | |
| Recruiting |
NCT05937542 -
A Qualitative Investigation of CLEAT Participants
|
||
| Completed |
NCT03644615 -
A Mindfulness Program (MBSR) in the Management of Symptomatic Hip and Knee Osteoarthritis
|
N/A | |
| Recruiting |
NCT06061367 -
Muscles Strength and Gait Parameteres After TKA
|
||
| Withdrawn |
NCT04976972 -
A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional Instrumentation
|
N/A | |
| Completed |
NCT05496205 -
A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT03850665 -
Comparison of Functional Outcome in Patients After Hip Arthroplasty Depending on Surgical Approach
|
N/A | |
| Completed |
NCT02826902 -
Effect of Anesthesia on Quality of Recovery in Patients Undergoing Correctional Tibial Osteotomy - A Randomized Controlled Trial
|
N/A | |
| Completed |
NCT04402502 -
Dynamic 4DCT to Examine Wrist Carpal Mechanics
|
N/A | |
| Completed |
NCT02923700 -
Leukocyte-rich PRP vs Leukocyte-poor PRP for the Treatment of Knee Cartilage Degeneration: a Randomized Controlled Trial
|
Phase 4 | |
| Completed |
NCT04564053 -
Study of Safety, Tolerability and Pharmacokinetics of LNA043 in Japanese Osteoarthritis Participants
|
Phase 1 | |
| Completed |
NCT05070871 -
A Clinical Trial Investigating the Effect of Salmon Bone Meal on Osteoarthritis Among Men and Women
|
N/A | |
| Not yet recruiting |
NCT05036174 -
Diphenhydramine Ointment for Knee Osteoarthritis
|
N/A | |
| Recruiting |
NCT02912429 -
Onlay vs. Inlay Patellofemoral Arthroplasty
|
N/A | |
| Recruiting |
NCT02666443 -
Low Dose Dexamethasone in Supraclavicular Blocks
|
N/A | |
| Active, not recruiting |
NCT02723929 -
Effects of tDCS and tUS on Pain Perception in OA of the Knee
|
||
| Withdrawn |
NCT02921594 -
Kinematic Comparison of Vanguard XP and Vanguard CR Total Knee Arthroplasties
|
N/A | |
| Terminated |
NCT02820766 -
Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting
|
N/A |