Exploring Massage Benefits for Arthritis of the Knee

Phase 2

Completed

• Conditions: Osteoarthritis of the Knee
• Interventions: Other: Massage 30 min sessions 1x/wk for 8 wks; Other: Massage 30 min 2x/wk x4 wks then 1x/wk x4 wks; Other: Massage 60 min 2x/wk for 4 wks then 1x/wk for 4 wks; Other: Massage 60 min session 1x/wk for 8 wks

• Registration Number: NCT00970008
• Lead Sponsor: University of Medicine and Dentistry of New Jersey

Brief Summary

In 2004, we conducted a pilot randomized, wait list controlled, trial (RCT) of massage therapy for OA of the knee in 68 subjects. That study, supported by CDC grant SIP-14-00, revealed the potential efficacy of Swedish massage therapy in the treatment of OA of the knee, with benefits of increased function and decreased pain persisting at least eight weeks following treatment cessation. The results of that trial, the first RCT of massage for OA, were published in the Archives of Internal Medicine in 2006 (See reference in More Information section). This current project builds on the design and findings of the pilot trial to determine the optimal dose and treatment regimen and provide longer term follow up. This project is a dual-site, randomized, dose-ranging trial to compare four dose/regimens in order to identify the optimal protocol for clinical practice.

The primary study hypothesis is that an eight (8) week course of Swedish massage therapy of one of the four proposed doses (by frequency and duration of massage treatment session) will be effective in reducing pain and improving function in patients with confirmed OA of the knee.

Detailed Description

A dual-site, randomized, dose-ranging trial to determine the role and practice parameters for massage in the standard clinical management of OA based on investigation of efficacy and mechanism of action. The study hypothesis is that an 8 week course of Swedish massage therapy will be effective in reducing pain and improving function in patients with confirmed OA of the knee. A future phase III trial is planned to test the optimal massage intervention identified in this study against a validated sham/control intervention, incorporating all pertinent outcome measures from the antecedent studies. In addition, this study will further the development of robust methodologies to test the efficacy of massage interventions in general. The research agenda advanced by the current study will culminate with the establishment of the proper place for massage therapy among standard treatment options for the millions of Americans suffering with osteoarthritis.

Study Timeline

• Study First Submitted: 2009-08-18
• Study First Submitted QC: 2009-08-31
• Study Start: 2009-09
• Study First Posted: 2009-09-02
• Primary Completion: 2011-07
• Study Completion: 2011-08
• Status Verified: 2015-04
• Last Update Submitted: 2015-05-01
• Last Update Posted: 2015-05-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 125

Inclusion Criteria

• 35 years of age or greater.

• Written confirmation of OA of the knee as provided by the participant's physician.

• Radiographically-established OA of the knee.

• Pre-randomization score of 40 to 90 on the Visual Analog Pain Scale (0-100 mm scale).

• Patients with bilateral knee involvement will have the more severely affected knee designated as the study knee.

• American College of Rheumatology defined OA of the knee:

  1. Knee pain
  2. Satisfaction of at least five of the following nine criteria:
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  1. Age greater than 50 years
  2. Stiffness < 30 minutes
  3. Crepitus
  4. Bony tenderness
  5. Bony enlargement
  6. No palpable warmth
  7. ESR < 40 mm/hr
  8. Rheumatoid Factor (RF) < 1:40

Exclusion Criteria

(no exclusion criterion may be present)

• Presence of rheumatoid arthritis, fibromyalgia, recurrent or active pseudo gout.
• Presence of cancer or other serious medical conditions.
• Signs or history of kidney or liver failure.
• Presence of asthma requiring the use of corticosteroid treatment.
• Use of oral corticosteroids within the past four weeks.
• Use of intra-articular knee depo-corticosteroids with the past three months.
• Use of intra-articular hyaluronate with the past six months.
• Arthroscopic surgery of the knee within the past year.
• Significant injury to the knee within the past six months.
• Presence of a rash or open wound over the knee.
• Unable to satisfy the treatment and follow-up requirements.
• Unable to provide written informed consent.
• Currently receiving massage therapy on a regular basis (at least twice a month).
• Knee replacement of study knee (ok if the knee not being studied has been replaced).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Massage 30 min sessions - 1x/wk for 8wks	Massage 30 min sessions 1x/wk for 8 wks	Swedish massage session of 30 minutes duration, once weekly for eight weeks over a eight (8) week period. Total intervention = 8 sessions for 240 minutes.
Massage 30 min - 2x wk for 4 wks & 1x wk for 4 wks	Massage 30 min 2x/wk x4 wks then 1x/wk x4 wks	Swedish massage session of 30 minutes duration, twice weekly for four weeks followed by once weekly for four weeks over a eight (8) week period. Total intervention = 12 sessions for 360 minutes.
Massage 60 min - 2x wk for 4 wks & 1x wkly for 4 wks	Massage 60 min 2x/wk for 4 wks then 1x/wk for 4 wks	Swedish massage session of 60 minutes duration, twice weekly for four weeks followed by once weekly for four weeks over a eight (8) week period. Total intervention = 12 sessions for 720 minutes.
Massage 60 min sessions - 1x/wk for 8 wks	Massage 60 min session 1x/wk for 8 wks	Swedish massage session of 60 minutes duration, once weekly for eight weeks over a eight (8) week period. Total intervention = 8 sessions for 480 minutes

Primary Outcome Measures

Name	Time	Method
Improvement in WOMAC (Western Ontario Multipurpose Arthritis Centers) Knee and Hip Osteoarthritis Index	Six (6) months

Secondary Outcome Measures

Name	Time	Method
Safety	Six (6) months
Improvement in range of motion as measured by a goniometer.	six (6) months
Reduction in pain as measured by the Visual Analog Scale (VAS) for pain.	Six (6) months
Improvement in physical function as measured by time in seconds to walk fifty (50) feet on a level straight surface.	six (6) months

Trial Locations

Locations (2)

Siegler Center for Integrative Medicine - Saint Barnabas Ambulatory Care Center; 🇺🇸 Livingston, New Jersey, United States

Yale-Griffin Prevention Research Center/Griffin Hospital; 🇺🇸 Derby, Connecticut, United States