search
Back to results

Group Acupuncture Therapy With Modified Yoga (GAPYOGA)

Primary Purpose

Chronic Neck Pain, Chronic Low Back Pain, Osteoarthritis Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Acupuncture Therapy Treatments
Yoga Therapy Sessions
Sponsored by
Icahn School of Medicine at Mount Sinai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Neck Pain focused on measuring Acupuncture therapy, Yoga therapy, Integrative medicine, Chronic pain, Underserved, Safety net setting

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients 21 years of age or older
  • Chronic pain (three months or more in duration) due to a qualifying diagnosis of back pain, neck pain, and/or osteoarthritis.
  • Eligible patients must be receiving primary care at a participating IFH or Montefiore Medical Group site
  • Participants must understand and be able to provide consent in English or Spanish
  • Reliable contact phone numbers must be available to facilitate scheduling,
  • Availability for up to 10 weekly consecutive treatments and
  • Availability for follow-up data collection at 24 weeks

Exclusion criteria:

  • Receipt of acupuncture treatment or yoga instruction/therapy in the 6 months prior to recruitment
  • Pregnancy
  • Severe psychiatric problems as assessed by the study team (e.g., chronic interpersonal problems, cognitive impairment or active psychosis that is uncontrolled by medication that precludes the ability to provide informed consent or complete the survey instruments)

Sites / Locations

  • Montefiore Family Health Center
  • Williamsbridge Family Practice Center
  • The Institute For Family Health

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment

Arm Description

Participants with chronic pain to receive acupuncture therapy treatments and yoga therapy sessions.

Outcomes

Primary Outcome Measures

Change in Brief Pain Inventory: Short Form
The BPI is a nine-item measure which that asks patients to indicate how their pain influences function: select aspects of their everyday life including mood, walking, sleep and their ability to work over the past 24 hours, as well as the level and intensity of pain. This measure will be adapted for use by phone, modifying a question which asks participants to refer to a diagram of the body. total score from 0 to 10, with higher score indicating worse outcomes.

Secondary Outcome Measures

Change in Pain Free Days
Self-report measure to report the number of pain free days in the previous 2 weeks. This measure will be used pre- and post-intervention.
Change in Center for Epidemiological Studies - Depression Scale (CES-D)
This is a well-validated, 20-item measure of depressive symptoms. This will be used both at the initiation treatment interview and the end of the study. Full score from 0- 20, with higher score indicating more symptomology.
Change in Altarum Consumer Engagement (ACE)
A 12-item measure that assesses three domains of health engagement: commitment, informed choice, and navigation. The measure covers areas not included in other surveys and it is a good predictor of current health status, lifestyle health behaviors, medication adherence, and how likely it is that people will use tools to support their decisions. This measure will be adapted to include 8 of the 12 items on the questionnaire. Full scale from 0-100, higher score indicates higher consumer engagement.
Change in Patient-Reported Outcomes Measurement Information System (PROMIS 10)
A series of person-centered measures that evaluate and monitor physical, mental, and social health in adults and children. 10-item patient-reported questionnaire. standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.
Change in PROMIS Satisfaction with Participation in Social Roles (PROMIS-SF)
is a 14-item measure that is part of the PROMIS Social Function. The measure refers to social roles, such as work and family responsibilities, and more discretionary social activities, such as leisure activity and relationships with friends. standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.
Change in Patient Global Impression of Change (PGIC)
Patient Global Impression of Change (PGIC) is a single question 7-point categorical scale that captures a patient's experience of treatment at follow-up points, after all sessions are completed. Full score from 0-7, with higher score indicating more improvement.
Change in Medication Utilization
Participants will be asked to report their use of pain medications over the prior one-week period.

Full Information

First Posted
March 3, 2020
Last Updated
February 1, 2021
Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
The Institute for Family Health, Albert Einstein College of Medicine, Maryland University of Integrative Health
search

1. Study Identification

Unique Protocol Identification Number
NCT04296344
Brief Title
Group Acupuncture Therapy With Modified Yoga
Acronym
GAPYOGA
Official Title
Group Acupuncture Therapy With Modified Yoga for Chronic Neck, Low Back and OA Pain in Safety Net Setting for an Underserved Population (GAPYOGA)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 8, 2019 (Actual)
Primary Completion Date
November 11, 2020 (Actual)
Study Completion Date
November 11, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai
Collaborators
The Institute for Family Health, Albert Einstein College of Medicine, Maryland University of Integrative Health

4. Oversight

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

5. Study Description

Brief Summary
Chronic pain is prevalent in the U.S., with impact on physical and psychological functioning as well as lost work productivity. Minority and lower socioeconomic populations have increased prevalence of chronic pain with less access to pain care and poorer outcomes. Acupuncture therapy is effective in treating chronic pain conditions including chronic low back pain (cLBP), neck pain, shoulder pain and knee pain from osteoarthritis (OA). Acupuncture therapy, including group acupuncture, is feasible and effective, and specifically so for underserved and diverse populations at risk for health outcome disparities. Acupuncture therapy also encourages patient engagement and activation. As chronic pain improves there is a natural progression to want and need to increase activity and movement recovery. Diverse movement approaches are important both for improving range of motion, maintaining gains, strengthening and promoting patient engagement and activation. Yoga therapy is an active therapy with proven benefit in musculoskeletal pain disorders and pain associated disability. The aim of this pilot feasibility trial is to test the bundling of these two care options for chronic pain, to inform both the design for a larger randomized pragmatic effectiveness trial as well as implementation strategies across underserved settings.
Detailed Description
The goal of this project is to assess the feasibility of a low-cost, integrative intervention for chronic pain that can be replicated and implemented in underserved medical settings across the U.S. Over the course of 18 months, the study team will recruit at least 150 outpatients with chronic pain from the Institute for Family Health (IFH) Family Medicine sites and Montefiore Medical Group sites, both Federally Qualified Health Centers (FQHCs). Treatment will consist of ten consecutive weekly group acupuncture therapy treatments. Yoga therapy treatments will start at week three and will consist of eight consecutive yoga therapy sessions that occur immediately following in a room adjacent to acupuncture therapy. Sessions are bundled to facilitate attendance that might be affected by two separate trips a week for participation. The primary outcome will be pain interference and pain intensity. Secondary outcomes will be pain free days, depression, functional status, patient activation, and pain medication utilization. These will be used during the pre-intervention phase, during which patients are receiving usual care only, and compared to the period after patients receive the combined acupuncture and yoga sessions. Data will be collected for 10 days before acupuncture and yoga therapy, and up to 24 weeks following the end of treatment. The study will use a 'multiple settings across baseline' quasi-experimental design. This is a repeated measures design, and each study participant will have multiple pre- and post-measures. The multiple pre-measurement points allows the study team to document and monitor what may be variable patterns of pain pre-intervention. This design optimizes feasibility and acceptability to patients and participating health centers while still generating meaningful outcome data. Specifically, the study team has not proposed randomization within the practices, rather allowing sites to offer the intervention to all patients with target diagnoses who meet eligibility criteria. To collect pre-acupuncture assessments of pain, the study team will include a 10 day intake run-in period prior to the initial acupuncture session that ensures treatment within a time frame that is consistent with typical time to appointments for many consultations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Neck Pain, Chronic Low Back Pain, Osteoarthritis Pain
Keywords
Acupuncture therapy, Yoga therapy, Integrative medicine, Chronic pain, Underserved, Safety net setting

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
94 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
Participants with chronic pain to receive acupuncture therapy treatments and yoga therapy sessions.
Intervention Type
Other
Intervention Name(s)
Acupuncture Therapy Treatments
Intervention Description
10 consecutive weekly group acupuncture therapy treatments
Intervention Type
Other
Intervention Name(s)
Yoga Therapy Sessions
Intervention Description
8 consecutive yoga therapy sessions that occur immediately following in a room adjacent to acupuncture therapy.
Primary Outcome Measure Information:
Title
Change in Brief Pain Inventory: Short Form
Description
The BPI is a nine-item measure which that asks patients to indicate how their pain influences function: select aspects of their everyday life including mood, walking, sleep and their ability to work over the past 24 hours, as well as the level and intensity of pain. This measure will be adapted for use by phone, modifying a question which asks participants to refer to a diagram of the body. total score from 0 to 10, with higher score indicating worse outcomes.
Time Frame
Baseline and Week 24
Secondary Outcome Measure Information:
Title
Change in Pain Free Days
Description
Self-report measure to report the number of pain free days in the previous 2 weeks. This measure will be used pre- and post-intervention.
Time Frame
Baseline and Week 24
Title
Change in Center for Epidemiological Studies - Depression Scale (CES-D)
Description
This is a well-validated, 20-item measure of depressive symptoms. This will be used both at the initiation treatment interview and the end of the study. Full score from 0- 20, with higher score indicating more symptomology.
Time Frame
Baseline and Week 24
Title
Change in Altarum Consumer Engagement (ACE)
Description
A 12-item measure that assesses three domains of health engagement: commitment, informed choice, and navigation. The measure covers areas not included in other surveys and it is a good predictor of current health status, lifestyle health behaviors, medication adherence, and how likely it is that people will use tools to support their decisions. This measure will be adapted to include 8 of the 12 items on the questionnaire. Full scale from 0-100, higher score indicates higher consumer engagement.
Time Frame
Baseline and Week 24
Title
Change in Patient-Reported Outcomes Measurement Information System (PROMIS 10)
Description
A series of person-centered measures that evaluate and monitor physical, mental, and social health in adults and children. 10-item patient-reported questionnaire. standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.
Time Frame
Baseline and Week 24
Title
Change in PROMIS Satisfaction with Participation in Social Roles (PROMIS-SF)
Description
is a 14-item measure that is part of the PROMIS Social Function. The measure refers to social roles, such as work and family responsibilities, and more discretionary social activities, such as leisure activity and relationships with friends. standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.
Time Frame
Baseline and Week 24
Title
Change in Patient Global Impression of Change (PGIC)
Description
Patient Global Impression of Change (PGIC) is a single question 7-point categorical scale that captures a patient's experience of treatment at follow-up points, after all sessions are completed. Full score from 0-7, with higher score indicating more improvement.
Time Frame
Week 10 and Week 24
Title
Change in Medication Utilization
Description
Participants will be asked to report their use of pain medications over the prior one-week period.
Time Frame
Baseline and Week 24

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients 21 years of age or older Chronic pain (three months or more in duration) due to a qualifying diagnosis of back pain, neck pain, and/or osteoarthritis. Eligible patients must be receiving primary care at a participating IFH or Montefiore Medical Group site Participants must understand and be able to provide consent in English or Spanish Reliable contact phone numbers must be available to facilitate scheduling, Availability for up to 10 weekly consecutive treatments and Availability for follow-up data collection at 24 weeks Exclusion criteria: Receipt of acupuncture treatment or yoga instruction/therapy in the 6 months prior to recruitment Pregnancy Severe psychiatric problems as assessed by the study team (e.g., chronic interpersonal problems, cognitive impairment or active psychosis that is uncontrolled by medication that precludes the ability to provide informed consent or complete the survey instruments)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raymond Teets, MD
Organizational Affiliation
MOUNT SINAI HOSPITAL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montefiore Family Health Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10458
Country
United States
Facility Name
Williamsbridge Family Practice Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10469
Country
United States
Facility Name
The Institute For Family Health
City
New York
State/Province
New York
ZIP/Postal Code
10035
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices).
IPD Sharing Time Frame
Beginning 3 months and ending 5 years following article publication.
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal.Any purpose.Proposals may be submitted up to 36 months following article publication. After 36 months the data will be available in our University's data warehouse but without investigator support other than deposited metadata. Information regarding submitting proposals and accessing data may be found at (Link to be provided).
Citations:
PubMed Identifier
33720749
Citation
Anderson BJ, Meissner P, Mah DM, Nielsen A, Moonaz S, McKee MD, Kligler B, Milanes M, Guerra H, Teets R. Barriers and Facilitators to Implementing Bundled Acupuncture and Yoga Therapy to Treat Chronic Pain in Community Healthcare Settings: A Feasibility Pilot. J Altern Complement Med. 2021 Jun;27(6):496-505. doi: 10.1089/acm.2020.0394. Epub 2021 Mar 15.
Results Reference
derived

Learn more about this trial

Group Acupuncture Therapy With Modified Yoga

We'll reach out to this number within 24 hrs