Periosteal Stimulation for Knee Osteoarthritis (PST)
Primary Purpose
Osteoarthritis, Knee
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Periosteal stimulation
Control-Periosteal Stimulation
Sponsored by

About this trial
This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring acupuncture
Eligibility Criteria
Inclusion Criteria:
- English speaking,
- Knee pain on most days of the past 3 months that is more severe than pain in other parts of the lower body,
- Advanced knee OA by x-ray,
- age 50-89
Exclusion Criteria:
- Non-ambulatory or severely impaired mobility (i.e., require the use of a walker),
- Folstein MMSE < 24,
- Severe uncorrected visual or hearing impairment,
- Knee pain due to factors other than OA,
- Large knee effusion,
- History of corticosteroid or hyaluronic acid injection in the affected knee(s) during the preceding 3 months,
- Acute or terminal illness,
- Immune suppression,
- Anticoagulation therapy,
- Pacemaker,
- Prior PST treatment
- Active participation in other studies currently
- Age >89
Sites / Locations
- Geriatric Research, Education, and Clinical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Placebo Comparator
Arm Label
PST + PST boosters
PST + control-PST boosters
Control-PST
Arm Description
PST once a week for 10 weeks, then tapering over 6 months
PST once a week for 10 weeks, then control-PST tapering over 6 months
control-PST for 10 weeks
Outcomes
Primary Outcome Measures
Pain (WOMAC)
The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) consists of 24 items divided into 3 subscales:
Pain (5 items), score range 0-20 Stiffness (2 items): score range 0-8 Physical Function (17 items): score range 0-68 Total score ranges from 0 (best possible outcome) to 96 (worst possible outcome)
Secondary Outcome Measures
Full Information
NCT ID
NCT00865046
First Posted
March 17, 2009
Last Updated
January 22, 2015
Sponsor
US Department of Veterans Affairs
1. Study Identification
Unique Protocol Identification Number
NCT00865046
Brief Title
Periosteal Stimulation for Knee Osteoarthritis
Acronym
PST
Official Title
Efficacy of Periosteal Stimulation and Boosters for Advanced Knee OA Pain
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
185 veterans with chronic knee pain and advanced knee osteoarthritis will be recruited to participate in this study designed to test the effectiveness of a special type of electrical acupuncture called periosteal stimulation (PST). Participants will be divided into three groups. They will receive PST or a control condition once a week for 10 weeks. Two-thirds of the participants will receive booster sessions periodically over the course of the next 6 months. Everyone will be called monthly during the 6 month period and then will be asked to return for an evaluation on site at the end of this period.
Detailed Description
We have performed a promising initial trial of periosteal stimulation (PST, that is, electrical stimulation of 4 acupuncture needles around the knee that touch periosteum) as an analgesic for older veterans with advanced knee osteoarthritis (OA) and daily pain. The primary aim of the proposed trial is to optimize and sustain the efficacy of PST for reducing pain in veterans with advanced knee OA and unrelieved pain by combining it with booster PST. Our secondary aims are to 1) improve physical performance in these individuals, and 2) ascertain the physical and psychological predictors of response to PST. In a randomized controlled clinical trial, 180 veterans (age 50 and older) with persistent knee pain who have x-ray evidence of advanced OA will be assigned to one of three intervention groups: 1) control PST once a week for 10 weeks (i.e., needle placement with brief stimulation of non-periosteal needles), 2) PST once a week for 10 weeks followed by tapering PST boosters over 6 months, or 3) PST once a week for 10 weeks followed by tapering control-PST boosters over 6 months. Prior to initiating the intervention, immediately after the last session, and 6 months later, the following parameters will be assessed: 1) pain severity (WOMAC), 3) physical performance (gait velocity, stair climb, repetitive chair rise, timed up and go), and 4) psychological function (mood, coping, self-efficacy). Monthly telephone calls will assess pain, interim illness and physical activity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
acupuncture
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
190 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PST + PST boosters
Arm Type
Experimental
Arm Description
PST once a week for 10 weeks, then tapering over 6 months
Arm Title
PST + control-PST boosters
Arm Type
Active Comparator
Arm Description
PST once a week for 10 weeks, then control-PST tapering over 6 months
Arm Title
Control-PST
Arm Type
Placebo Comparator
Arm Description
control-PST for 10 weeks
Intervention Type
Other
Intervention Name(s)
Periosteal stimulation
Intervention Description
Four acupuncture needles are placed around the knee to the level of the periosteum and two needles are placed pretibially in the soft tissue. All needles are stimulated with 100 Hz current. The stimulation of the needles in the soft tissue is discontinued after one minute.
Intervention Type
Other
Intervention Name(s)
Control-Periosteal Stimulation
Intervention Description
Acupuncture needles are placed as per the PST intervention, but only the soft tissue needles receive electrical stimulation for one minute.
Primary Outcome Measure Information:
Title
Pain (WOMAC)
Description
The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) consists of 24 items divided into 3 subscales:
Pain (5 items), score range 0-20 Stiffness (2 items): score range 0-8 Physical Function (17 items): score range 0-68 Total score ranges from 0 (best possible outcome) to 96 (worst possible outcome)
Time Frame
9 months following baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
English speaking,
Knee pain on most days of the past 3 months that is more severe than pain in other parts of the lower body,
Advanced knee OA by x-ray,
age 50-89
Exclusion Criteria:
Non-ambulatory or severely impaired mobility (i.e., require the use of a walker),
Folstein MMSE < 24,
Severe uncorrected visual or hearing impairment,
Knee pain due to factors other than OA,
Large knee effusion,
History of corticosteroid or hyaluronic acid injection in the affected knee(s) during the preceding 3 months,
Acute or terminal illness,
Immune suppression,
Anticoagulation therapy,
Pacemaker,
Prior PST treatment
Active participation in other studies currently
Age >89
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Debra K. Weiner, MD
Organizational Affiliation
Geriatric Research, Education, and Clinical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Geriatric Research, Education, and Clinical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15206
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24184053
Citation
Weiner DK, Moore CG, Morone NE, Lee ES, Kent Kwoh C. Efficacy of periosteal stimulation for chronic pain associated with advanced knee osteoarthritis: a randomized, controlled clinical trial. Clin Ther. 2013 Nov;35(11):1703-20.e5. doi: 10.1016/j.clinthera.2013.09.025. Epub 2013 Nov 1.
Results Reference
result
Learn more about this trial
Periosteal Stimulation for Knee Osteoarthritis
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