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Comparing Different Types of Physical Therapy for Treating People With a Meniscal Tear and Osteoarthritis (TeMPO)

Primary Purpose

Meniscal Degeneration, Osteoarthritis, Knee

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
TeMPO Home Exercise Program
Motivational SMS Messages
In-Clinic Topical Therapy
In-Clinic Exercise Therapy
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Meniscal Degeneration focused on measuring physical therapy

Eligibility Criteria

45 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Knee pain of at least 21 days duration if traumatic; no minimum duration if non-traumatic
  • Age 45 -85 years
  • Physician diagnosis of meniscal tear
  • Evidence on MRI of meniscal tear
  • Evidence of osteoarthritic changes on imaging: Cartilage damage on MRI, osteophyte or joint space narrowing on X-ray

Exclusion Criteria:

  • KL-Grade 4
  • Inflammatory arthritis
  • Prior APM or TKR on index knee; or any surgery on index knee in prior 6 mo
  • Pregnancy
  • Contraindication to MRI
  • Daily use of strong opioids
  • Intra-articular therapy in last 4 weeks
  • Non-English speaking
  • History of dementia
  • Currently resides in a nursing home
  • Current claimant of worker's compensation for this condition

Sites / Locations

  • Brigham and Women's HospitalRecruiting
  • University at Buffalo Medical DepartmentRecruiting
  • Cleveland ClinicRecruiting
  • University of Pittsburgh Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

1. Home Exercise Program

2. Home Exercise Program + SMS Messages

3. In-Clinic Topical Therapy

4. In-Clinic Exercise Therapy

Arm Description

The Home Exercise group receives the TeMPO Home Exercise Program (including a set of weights, a DVD showing how to complete the TeMPO exercises, and a pamphlet outlining instructions on how to complete the exercises and how often should they be done).

Subjects in this arm receive the TeMPO Home Exercise Program and motivational SMS messages to encourage them to adhere to the TeMPO Home Exercise regimen.

Subjects in this arm receive the TeMPO Home Exercise Program, motivational SMS messages to encourage them to adhere to the TeMPO Home Exercise Program, and 14 in-clinic sessions with a trained physical therapist. The therapist will apply topical therapies: ultrasound, gel, and manual therapy.

Subjects in this arm will receive the TeMPO Home Exercise Program, SMS motivational messages to encourage them to adhere to the TeMPO Home Exercise Program and 14 in-clinic sessions with a trained physical therapist. The therapist will supervise the participant in a rigorous set of strengthening and stretching exercises.

Outcomes

Primary Outcome Measures

Change in Pain
Difference between arms in change in the KOOS Pain score over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1. Arm 4 vs. Arm 3)

Secondary Outcome Measures

Change in function
Difference between arms in change in the KOOS ADL score over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Change in quality of life
Difference between arms in change in quality of life measured with the EQ-5D scale over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Binary treatment failure indicator
Difference between arms in treatment failure defined as either not reaching improvement of >=8 points on KOOS Pain or receiving injection or undergoing index knee surgery within three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Forty meter fast-paced walk
Difference between arms in change in 40 m fast-paced walk (seconds) over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
30-second sit to stand
Difference between arms in number of repetitions (of sit to stand) over 30 seconds
Strength of quadriceps, hamstrings, gluteus medius
Difference between arms in strength (pounds-cm) between arms, measured at three sites (quadriceps, hamstrings, gluteus medius)
Single Leg Balance
Difference between arms in number of seconds participant can stand on single leg without moving hands off hips, stepping or stumbling, abducting or flexing hip beyond 30 deg, lifting heel or forefoot off ground.
Durability of pain relief
Difference between arms in proportion of subjects who maintain through 12 months the benefit (in KOOS Pain) achieved at 3 months. (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3 )

Full Information

First Posted
February 14, 2017
Last Updated
September 13, 2022
Sponsor
Brigham and Women's Hospital
Collaborators
National Institutes of Health (NIH), State University of New York at Buffalo, The Cleveland Clinic, University of Pittsburgh, University of Melbourne, Boston University
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1. Study Identification

Unique Protocol Identification Number
NCT03059004
Brief Title
Comparing Different Types of Physical Therapy for Treating People With a Meniscal Tear and Osteoarthritis
Acronym
TeMPO
Official Title
Treatment of Meniscal Problems in Osteoarthritis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 6, 2018 (Actual)
Primary Completion Date
January 1, 2023 (Anticipated)
Study Completion Date
March 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
National Institutes of Health (NIH), State University of New York at Buffalo, The Cleveland Clinic, University of Pittsburgh, University of Melbourne, Boston University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Knee osteoarthritis is a disabling problem affecting over 15 million adults in the United States. Many people who have knee arthritis also experience painful meniscal tears. There are a number of different treatments that can be used to manage meniscal tears in the presence of knee arthritis. Treatments include surgically removing the damaged part of the meniscus; strengthening exercises to improve pain and function; manual therapy including massage and mobilization; acupuncture; and others. The combination of surgery and exercise therapy was long thought to be the best treatment. However, recent studies have shown that surgery followed by physical therapy is no more effective than physical therapy by itself. While physical therapy alone has been shown to result in similar pain relief as arthroscopic surgery, researchers have not yet done studies to determine what type of physical therapy is best for people with knee arthritis and meniscal tears. In the "TeMPO" Trial, we will be comparing 4 different, non-operative physical therapy regimens in order to gain a better understanding of how physical therapy works and what regimen will best reduce pain and improve function in persons with meniscal tear and osteoarthritis. The four arms in this randomized trial will contain different combinations of therapeutic treatments including in-clinic therapist-supervised exercise, in-clinic topical therapies, and exercises to be completed at home. Subjects in three of the arms will also receive motivational SMS (text) messages intended to improve adherence to the home exercise regimen. TeMPO is designed as a randomized controlled trial. Participants will be assigned randomly to one of the four arms. All arms include therapies that have been previously shown to work in clinical settings. One arm also contains some placebo treatments. The placebo treatments will help us to understand what aspects of physical therapy actually make people feel better. Our hypothesis is that subjects in the arm that includes in-clinic physical therapy and a home exercise regimen will experience more pain relief than subjects in each of the other arms. Also, we expect that subjects in the arm that receives the home exercise regimen and SMS messages will experience more pain relief than subjects in the arm that receives home exercise without the SMS messages.
Detailed Description
Knee osteoarthritis is a disabling problem affecting over 15 million adults in the United States. Many people who have knee arthritis also experience painful meniscal tears. There are a number of different treatments that can be used to address meniscal tears in the presence of knee arthritis. These include surgically removing the damaged part of the meniscus; strengthening exercises; manual therapy including massage and mobilization; and others. The combination of surgery and exercise therapy was long thought to be the best treatment. However, recent studies have shown that surgery followed by physical therapy leads to similar levels of pain relief as physical therapy alone. While physical therapy appears to be useful in knee osteoarthritis and meniscal tear, research is needed to determine what type of physical therapy is best for people with these conditions. The "TeMPO" Trial will compare 4 different non-operative regimens in order to gain a better understanding of how physical therapy works and to determine which regimen will best reduce participants' pain and improve their function. The four arms in this trial will contain different combinations of therapeutic treatments including in-clinic supervised exercise therapy, in-clinic topical therapies, and exercises to be completed at home. Some of the arms will also receive text messages designed to improve adherence to assigned exercises. All arms include therapies that have been previously shown to work in clinical settings. One arm also contains some placebo treatments. The placebo treatments will help identify the aspects of physical therapy that make people feel better. The four arms in the TeMPO study are as follows: Home Exercise Program Home Exercise Program + Motivational SMS messages Home Exercise Program + Motivational SMS messages + In-Clinic topical therapy Home Exercise Program + Motivational SMS messages + In-Clinic Exercise Therapy

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Meniscal Degeneration, Osteoarthritis, Knee
Keywords
physical therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Four arm parallel randomized controlled trial.
Masking
Outcomes Assessor
Masking Description
Outcomes assessors will not be appraised of treatment arm.
Allocation
Randomized
Enrollment
860 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1. Home Exercise Program
Arm Type
Experimental
Arm Description
The Home Exercise group receives the TeMPO Home Exercise Program (including a set of weights, a DVD showing how to complete the TeMPO exercises, and a pamphlet outlining instructions on how to complete the exercises and how often should they be done).
Arm Title
2. Home Exercise Program + SMS Messages
Arm Type
Experimental
Arm Description
Subjects in this arm receive the TeMPO Home Exercise Program and motivational SMS messages to encourage them to adhere to the TeMPO Home Exercise regimen.
Arm Title
3. In-Clinic Topical Therapy
Arm Type
Experimental
Arm Description
Subjects in this arm receive the TeMPO Home Exercise Program, motivational SMS messages to encourage them to adhere to the TeMPO Home Exercise Program, and 14 in-clinic sessions with a trained physical therapist. The therapist will apply topical therapies: ultrasound, gel, and manual therapy.
Arm Title
4. In-Clinic Exercise Therapy
Arm Type
Experimental
Arm Description
Subjects in this arm will receive the TeMPO Home Exercise Program, SMS motivational messages to encourage them to adhere to the TeMPO Home Exercise Program and 14 in-clinic sessions with a trained physical therapist. The therapist will supervise the participant in a rigorous set of strengthening and stretching exercises.
Intervention Type
Behavioral
Intervention Name(s)
TeMPO Home Exercise Program
Intervention Description
This exercise program includes quadriceps, gluteus medius, gluteus maximus, and core exercises. The program includes a DVD and multi-page instruction pamphlet.
Intervention Type
Behavioral
Intervention Name(s)
Motivational SMS Messages
Intervention Description
The motivational SMS messages will be sent three times per week encouraging participants to complete their exercises.
Intervention Type
Behavioral
Intervention Name(s)
In-Clinic Topical Therapy
Intervention Description
Subjects will be assigned to a physical therapist and will attend 14 in-clinic topical therapy sessions. Sessions will include application of ultrasound, gel, and manual therapy.
Intervention Type
Behavioral
Intervention Name(s)
In-Clinic Exercise Therapy
Intervention Description
Subjects will be assigned to a physical therapist and will attend 14 in-clinic exercise and manual therapy sessions. Sessions will include the same exercises from the Home Exercise Program but the in-clinic therapy setting will allow for more personalization.
Primary Outcome Measure Information:
Title
Change in Pain
Description
Difference between arms in change in the KOOS Pain score over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1. Arm 4 vs. Arm 3)
Time Frame
Randomization to 3 months
Secondary Outcome Measure Information:
Title
Change in function
Description
Difference between arms in change in the KOOS ADL score over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Time Frame
Randomization to 3 months
Title
Change in quality of life
Description
Difference between arms in change in quality of life measured with the EQ-5D scale over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Time Frame
Randomization to 3 months
Title
Binary treatment failure indicator
Description
Difference between arms in treatment failure defined as either not reaching improvement of >=8 points on KOOS Pain or receiving injection or undergoing index knee surgery within three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Time Frame
Randomization to 3 months
Title
Forty meter fast-paced walk
Description
Difference between arms in change in 40 m fast-paced walk (seconds) over three months (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3)
Time Frame
Randomization to 3 months
Title
30-second sit to stand
Description
Difference between arms in number of repetitions (of sit to stand) over 30 seconds
Time Frame
Randomization to 3 months
Title
Strength of quadriceps, hamstrings, gluteus medius
Description
Difference between arms in strength (pounds-cm) between arms, measured at three sites (quadriceps, hamstrings, gluteus medius)
Time Frame
Baseline to 3 months
Title
Single Leg Balance
Description
Difference between arms in number of seconds participant can stand on single leg without moving hands off hips, stepping or stumbling, abducting or flexing hip beyond 30 deg, lifting heel or forefoot off ground.
Time Frame
Baseline to 3 months
Title
Durability of pain relief
Description
Difference between arms in proportion of subjects who maintain through 12 months the benefit (in KOOS Pain) achieved at 3 months. (Arm 4 vs. Arm 1; Arm 4 vs. Arm 2; Arm 2 vs. Arm 1; Arm 4 vs. Arm 3 )
Time Frame
3-12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Knee pain of at least 21 days duration if traumatic; no minimum duration if non-traumatic Age 45 -85 years Physician diagnosis of meniscal tear Evidence on MRI of meniscal tear Evidence of osteoarthritic changes on imaging: Cartilage damage on MRI, osteophyte or joint space narrowing on X-ray Exclusion Criteria: KL-Grade 4 Inflammatory arthritis Prior APM or TKR on index knee; or any surgery on index knee in prior 6 mo Pregnancy Contraindication to MRI Daily use of strong opioids Intra-articular therapy in last 4 weeks Non-English speaking History of dementia Currently resides in a nursing home Current claimant of worker's compensation for this condition
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jeffrey N Katz, MD, MSc
Phone
6177325338
Email
jnkatz@partners.org
First Name & Middle Initial & Last Name or Official Title & Degree
Faith Selzer, PhD
Phone
6175258301
Email
fselzer@partners.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chuck Washabaugh, PhD
Organizational Affiliation
National Institute for Arthritis, Musculoskeletal and Skin Diseases (NIAMS, NIH)
Official's Role
Study Chair
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Faith Selzer, PhD
Phone
617-525-8617
Email
fselzer@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Kaetlyn R Arant, BA
Phone
617 732 4313
Email
karant@bwh.harvard.edu
First Name & Middle Initial & Last Name & Degree
Jeffrey N Katz, MD
Facility Name
University at Buffalo Medical Department
City
Buffalo
State/Province
New York
ZIP/Postal Code
14215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melissa Kluczynski, MS
Phone
716-829-2561
Email
mk67@buffalo.edu
First Name & Middle Initial & Last Name & Degree
Leslie Bisson, MD
First Name & Middle Initial & Last Name & Degree
John Leddy, MD
Facility Name
Cleveland Clinic
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jen Turczyk
Phone
216-444-2924
Email
turczyk@ccf.org
First Name & Middle Initial & Last Name & Degree
Morgan Jones, MD, MPH
First Name & Middle Initial & Last Name & Degree
Kurt Spindler, MD
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15237
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bryan Galvin
Phone
412-432-3619
Email
bryan.galvin@chp.edu
First Name & Middle Initial & Last Name & Degree
Jay Irrgang, PhD, PT
First Name & Middle Initial & Last Name & Degree
Aaron Mares, MD
First Name & Middle Initial & Last Name & Degree
Ale Gil, PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31684921
Citation
Safran-Norton CE, Sullivan JK, Irrgang JJ, Kerman HM, Bennell KL, Calabrese G, Dechaves L, Deluca B, Gil AB, Kale M, Luc-Harkey B, Selzer F, Sople D, Tonsoline P, Losina E, Katz JN. A consensus-based process identifying physical therapy and exercise treatments for patients with degenerative meniscal tears and knee OA: the TeMPO physical therapy interventions and home exercise program. BMC Musculoskelet Disord. 2019 Nov 4;20(1):514. doi: 10.1186/s12891-019-2872-x.
Results Reference
derived
PubMed Identifier
30501629
Citation
Sullivan JK, Irrgang JJ, Losina E, Safran-Norton C, Collins J, Shrestha S, Selzer F, Bennell K, Bisson L, Chen AT, Dawson CK, Gil AB, Jones MH, Kluczynski MA, Lafferty K, Lange J, Lape EC, Leddy J, Mares AV, Spindler K, Turczyk J, Katz JN. The TeMPO trial (treatment of meniscal tears in osteoarthritis): rationale and design features for a four arm randomized controlled clinical trial. BMC Musculoskelet Disord. 2018 Dec 1;19(1):429. doi: 10.1186/s12891-018-2327-9.
Results Reference
derived

Learn more about this trial

Comparing Different Types of Physical Therapy for Treating People With a Meniscal Tear and Osteoarthritis

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