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Physical Therapy Integrated With Mindfulness for Patients With Chronic Pain and Opioid Treatment (PT-IN-MIND)

Primary Purpose

Chronic Pain, Pain, Musculoskeletal, Opioid Use

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mindfulness based practice
Control/Standard Physical Therapy
Sponsored by
University of Utah
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Chronic Pain

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Aim 1 Physical Therapist Inclusion Criteria: Employed at least .5 (Full Time Equivalent) Manages patients with musculoskeletal conditions Exclusion Criteria: None Aim 2 and 3 Physical Therapist Inclusion Criteria: Employed at least .5 (Full Time Equivalent) Manages patients with musculoskeletal conditions Physical Therapist Exclusion Criteria: -Attended any experiential (i.e., practice sessions with real or simulated patients) mindfulness training to be used for patient care Attended any patient care specific mindfulness training lasting more than 3 hours. Self-report using mindfulness interventions such as savoring and cognitive reappraisal (core components of MORE) as a primary intervention strategy for the majority of their caseload for patients with chronic musculoskeletal pain. Aims 1, 2 and 3 Patient Inclusion Criteria: Age 18-75 English Speaking Diagnosis of musculoskeletal pain condition involving the spine and/or peripheral joint(s) Current musculoskeletal pain present for greater than or equal to 3 months. Use of prescription opioids for most of the last 90 days (self-report) Patient Exclusion Criteria: Currently pregnant Currently receiving mind-body treatment for musculoskeletal pain from a healthcare provider (e.g. PT, chiropractic, massage therapy, etc) Currently receiving treatment for substance use disorder Musculoskeletal pain condition related to a fracture or surgical procedure in the past 6 months.

Sites / Locations

  • University of FloridaRecruiting
  • University of UtahRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Other

Experimental

Arm Label

Evidence based physical therapy combined with mindfulness (Low-Intensity)

Standard physical therapy

Evidence based physical therapy combined with mindfulness (High-Intensity)

Arm Description

Physical therapists randomized to this arm will receive a manual on how to integrate MORE; mindfulness, mindful reappraisal, and mindful savoring savoring into routine outpatient physical therapy for patients with chronic musculoskeletal pain and long-term opioid treatment. After 4 weeks to review the manual, the physical therapist's competency will be assessed during mock patient encounters using trained actors as standardized patients. Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about pain and opioid use before, and after treatment. We plan on enrolling 2 patients for each physical therapist.

Physical therapists randomized to this arm will deliver routine treatment for someone with chronic musculoskeletal pain and long-term opioid treatment. Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about pain and opioid use before, during and after treatment. We plan on enrolling 2 patients for each physical therapist.

Physical therapists randomized to this arm will receive 13 hours of training. The first 6 hours consists of prerecorded didactic lectures that the physical therapist can view on their own time. After viewing the lectures, participants will attend 6.25 hours of live experiential instruction to promote trainee competence in providing mindfulness, mindful reappraisal, and mindful savoring after which the participating physical therapist's competency will be assessed during mock patient encounters using trained actors as standardized patients. . Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about pain and opioid use before, and after treatment. We plan on enrolling 2 patients for each physical therapist.

Outcomes

Primary Outcome Measures

Aim #2: Mindfulness Oriented Recovery Enhancement fidelity measure
Mindfulness Oriented Recovery Enhancement fidelity (Modified MORE-FM) Version 2.0 measure score during post-training competency assessment of physical therapists (physical therapists randomized to High and Low Intensity training groups) 21-item scale - total scores range from 0 - 114. Scores are summed and averaged.
Aim #2: Opioid Dose on Timeline followback
Patient reported opioid dose on the timeline followback
Aim 3: PEG (Pain, Enjoyment, General activity)
The Pain, Enjoyment and General Active scale measures pain intensity, enjoyment of life and general activity each on a 0 - 10 with higher scores indicating worse pain impact. The score is the average of all items.
Aim #3 Opioid Dose on Timeline followback
Patient reported opioid dose on the timeline followback
Aim 3: PEG (Pain, Enjoyment, General Activity)
The Pain, Enjoyment and General Active scale measures pain intensity, enjoyment of life and general activity each on a 0 - 10 with higher scores indicating worse pain impact. The score is the average of all items.

Secondary Outcome Measures

Aim #1 Qualitative Interviews
Semi-structured qualitative interviews will be conducted with patients and physical therapists after they review a mindfulness treatment protocol. Analysis will generate qualitative themes that will be used to modify the treatment protocol in preparation for Aim #2.
Aim #2: Physical therapist retention (competency assessment)
Percent of physical therapists who attend the competency assessment.
Aim #2: Randomized physical therapists
Percentage of physical therapists invited who consent to be randomized
Aim #2: Physical therapist enrollment
Percent of physical therapists presented the study who choose to enroll in the study
Aim #3 Patient Reported: Patient Reported Outcomes Measurement Information System (PROMIS) Physical Function Short Form 6b (PROMIS-6b)
Reported as a T-Score with a mean of 50 and a SD of 10
Aim #3 Patient Reported:Patient Reported Outcomes Measurement Information System (PROMIS)PROMIS Sleep Disturbance Short Form 6a
Reported as a T-Score with a mean = 50 and a SD = 10
Aim #3 Patient Reported: Pain Catastrophizing Scale short form
Scores range 0- 24. Higher scores mean greater catastrophizing.
Aim #3 Patient Reported: Patient Health Questionnaire-2 (PHQ-2)
Scores range from 0-6. Higher scores mean greater likelihood of depression
Aim #3 Patient Reported: Generalized Anxiety Disorder-2 (GAD-2)
2 items summed range 0 - 6. Higher score mean greater likelihood of anxiety
Aim #3 Patient Reported: Patient Global Impression Scale-Change
Scores range from 0 - 7 with higher score equating to greater improvement in condition
Aim #3 Patient Reported: Pain Self-Efficacy Questionnaire
Scores range from0 - 60 with higher scores indicating greater levels of confidence in dealing with pain
Aim #3 Patient Reported: Mindfulness-Five Facet Mindfulness Questionnaire (FFMQ)
15 items scores range from 15 - 75 higher scores indicate greater mindfulness
Aim #3 Patient Reported: Positive Reappraisal Subscale of Cognitive Emotion Regulation Questionnaire
4 items each scored 1 - 5. Higher the score the more positive reappraisal.
Aim #3 Patient Reported: Savoring Beliefs Inventory
24 items. Composite scores are obtained by averaging the subscales after rescoring the negatively worded items. Higher scores equate to greater savoring.
Aim #3 Patient Reported: Participant-report health care utilization measures
Measure health care use (imaging, physician visits, medications)
Aim #3 Patient Reported: Short Assessment of Patient Satisfaction
7 items. Each item scored 0 - 4 . Reverse score items 1, 3, 5 and 7. Sum scores. Range from 0 (extremely dissatisfied to 7 (extremely satisfied)
Aim #3 Patient Reported: The Internal Pain Activity Questionnaire (IPAQ) short form measures physical activity
7 items. Measures metabolic equivalents (METS). Higher score in METS equates to greater activity.
Aim #3 Reach: Patients offered and enrolled
The percentage of patients with chronic muscle pain and long-term opioid treatment offered participation who choose to enroll.
Aim #3 Reach: Physical therapists with enrolled patients
The percentage of physical therapists who have a patient enrolled on their schedule
Aim #3 Effectiveness: REDCap Outcomes Collected
The percentage of outcomes collection using REDCap
Aim #3 Effectiveness: Timeline Follow Back
Percentage of Timeline Followback collected
Aim #3 Adoption: Qualitative interviews
Semi-structured qualitative interviews will be conducted with patient, PT, support staff interviews regarding their lived experience integrating mindfulness and physical therapy. Analysis will generate qualitative themes that will be used to plan for a fully-powered trial.
Aim #3 Adoption: Mindfulness Oriented Recovery Enhancement component (MORE)
Percentage of patients enrolled after I-EPT training that report receiving any MORE component.
Aim #3 Implementation: Fidelity
Mindfulness Oriented Recovery Enhancement _functional measure (Modified MORE-FM) fidelity measure during patient encounters. 21-item scale - total scores range from 0 - 114. Scores are summed and averaged.
Aim #3 Implementation: Qualitative Interviews
Semi-structured qualitative interviews will be conducted with patient, PT, support staff interviews regarding their lived experience integrating mindfulness and physical therapy. Analysis will generate qualitative themes that will be used to plan for a fully-powered trial.
Aim #3 Implementation: Percentage of patients managed by PT
The percentage of patients managed by a single trained physical therapist (don't cross over between physical therapists)
Aim #3: Maintenance: Qualitative Interviews
Semi-structured qualitative interviews will be conducted with patient, PT, support staff interviews regarding their lived experience integrating mindfulness and physical therapy. Analysis will generate qualitative themes that will be used to plan for a fully-powered trial. These interviews will be used to understand potential barriers for future implementation of physical therapy integrated with mindfulness
Aim #3: Physical therapist retention
The percentage of physical therapists who participate in the fidelity assessments
Aim #3: Patient retention
Percentage of patients managed by study physical therapists who are retained at baseline, 6- and 12-week follow-up.
Aim #3: Screened patients
Percentage of patients screened who are eligible
Sleep duration
hours and minutes of actual sleep during past month

Full Information

First Posted
April 12, 2023
Last Updated
August 28, 2023
Sponsor
University of Utah
Collaborators
University of Florida, National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT05875207
Brief Title
Physical Therapy Integrated With Mindfulness for Patients With Chronic Pain and Opioid Treatment
Acronym
PT-IN-MIND
Official Title
Physical Therapy Integrated With Mindfulness for Patients With Chronic Musculoskeletal Pain and Long-Term Opioid Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 14, 2023 (Actual)
Primary Completion Date
November 30, 2024 (Anticipated)
Study Completion Date
November 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Utah
Collaborators
University of Florida, National Center for Complementary and Integrative Health (NCCIH)

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
This study will use multiple methods to assess the feasibility of conducting a fully powered multisite clinical trial to test the effectiveness of integrating mindfulness-based interventions into physical therapy for patients with chronic musculoskeletal pain and long-term opioid treatment. First, researchers will develop a manual for training physical therapists to provide mindfulness-based interventions to patients with chronic musculoskeletal pain and long-term opioid treatment. Next, the researchers will evaluate the competency of physical therapists to provided mindfulness-based interventions after being randomized to one of 3 different mindfulness training arms. Patients scheduled for physical therapy with the randomized physical therapists will be invited to enroll in the study. These patients will be asked to complete a variety of patient reported outcomes including self-reported average pain and the the amount of prescription opioid pain medication taken.
Detailed Description
Chronic musculoskeletal pain is a leading cause of years lived with disability world-wide and the costliest health condition in the United States. An estimated 20%-30% of persons with chronic musculoskeletal pain use opioids for pain management. In recent years, the prevalence of long-term opioid treatment (LTOT) has increased in patients with musculoskeletal pain. Physical therapy (PT) is a common nonpharmacologic treatment recommended for chronic musculoskeletal pain. Studies suggest PT for musculoskeletal pain may reduce the likelihood of initiating opioid therapy and may protect against LTOT, but the role of PT as part of a multi-modal strategy to manage patients with chronic musculoskeletal pain and LTOT has not been investigated. Combining exercise-based interventions with mindfulness practices is effective for patients with chronic musculoskeletal pain, and engaging in mindfulness practices leads to a reduction in opioid dose in patients with chronic pain and LTOT. This is a feasibility study that will assess effectiveness of physical therapists in managing patients with chronic musculoskeletal pain and LTOT using mindfulness practices. the results of an aim may result in changes to the procedures of a subsequent aim. This study is organized into three Aims that will be conducted consecutively. Aim #1: is to refine and manualize physical therapist-led mindfulness-based interventions integrated with evidence-based PT (I-EPT) for patients with chronic musculoskeletal pain and LTOT. Our approach will use semi-structured interviews of 15 patients and 15 physical therapists to refine I-EPT. Aim #2: Evaluate different intensities of a physical therapist training programs for the refined I-EPT treatment protocol. Our approach will be to randomize 45 physical therapists to 1 of 3 training arms (no training; low-intensity training; high-intensity training). Aim #3: Evaluate the feasibility of the I-EPT intervention across domains of the RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) framework. We anticipate 90 patient participants will be enrolled onto the schedules of the randomized physical therapists in Aim 2. Semi-structured qualitative interviews will be conducted. For these interviews there will be separate cohorts of 27 participants from Utah and 27 from Florida. Each cohort will contain approximately 8 physical therapists (4 each from the HIghIT and LowIT programs), 13 patients and 7 between support staff, and clinic managers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain, Pain, Musculoskeletal, Opioid Use, Physical Therapy

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a multi-site feasibility randomized clinical trial.
Masking
Investigator
Masking Description
Lead statistician is also masked
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Evidence based physical therapy combined with mindfulness (Low-Intensity)
Arm Type
Experimental
Arm Description
Physical therapists randomized to this arm will receive a manual on how to integrate MORE; mindfulness, mindful reappraisal, and mindful savoring savoring into routine outpatient physical therapy for patients with chronic musculoskeletal pain and long-term opioid treatment. After 4 weeks to review the manual, the physical therapist's competency will be assessed during mock patient encounters using trained actors as standardized patients. Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about pain and opioid use before, and after treatment. We plan on enrolling 2 patients for each physical therapist.
Arm Title
Standard physical therapy
Arm Type
Other
Arm Description
Physical therapists randomized to this arm will deliver routine treatment for someone with chronic musculoskeletal pain and long-term opioid treatment. Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about pain and opioid use before, during and after treatment. We plan on enrolling 2 patients for each physical therapist.
Arm Title
Evidence based physical therapy combined with mindfulness (High-Intensity)
Arm Type
Experimental
Arm Description
Physical therapists randomized to this arm will receive 13 hours of training. The first 6 hours consists of prerecorded didactic lectures that the physical therapist can view on their own time. After viewing the lectures, participants will attend 6.25 hours of live experiential instruction to promote trainee competence in providing mindfulness, mindful reappraisal, and mindful savoring after which the participating physical therapist's competency will be assessed during mock patient encounters using trained actors as standardized patients. . Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about pain and opioid use before, and after treatment. We plan on enrolling 2 patients for each physical therapist.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness based practice
Intervention Description
Physical therapists who are randomized to this arm will receive mindfulness training. This training will teach physical therapists to use the following with their patients: 1) use mindfulness to strengthen self-regulation of habitual and compulsive opioid use, and to mitigate pain by reinterpreting these experiences as innocuous sensory information, 2) use reappraisal to reframe stressors and maladaptive thoughts to decrease negative emotions and engender meaning in life, 3) use savoring of pleasant events and pleasurable sensations to enhance positive emotions and reward and, 4) to integrate mindfulness, reappraisal and savoring with evidence-based physical therapy.
Intervention Type
Behavioral
Intervention Name(s)
Control/Standard Physical Therapy
Intervention Description
Physical therapists randomized to this arm will receive no additional training and will provide standard care to patients with chronic musculoskeletal pain and long-term opioid treatment. Patients with chronic musculoskeletal pain and long-term opioid treatment who seek care from a physical therapist in this arm will be approached to participate in the study. If eligible and willing to participate in the study they will be asked questions about their pain and opioid use before and after treatment. We plan on enrolling 2 patients for each physical therapist.
Primary Outcome Measure Information:
Title
Aim #2: Mindfulness Oriented Recovery Enhancement fidelity measure
Description
Mindfulness Oriented Recovery Enhancement fidelity (Modified MORE-FM) Version 2.0 measure score during post-training competency assessment of physical therapists (physical therapists randomized to High and Low Intensity training groups) 21-item scale - total scores range from 0 - 114. Scores are summed and averaged.
Time Frame
6 weeks
Title
Aim #2: Opioid Dose on Timeline followback
Description
Patient reported opioid dose on the timeline followback
Time Frame
Change in opioid dose from baseline to 6 weeks
Title
Aim 3: PEG (Pain, Enjoyment, General activity)
Description
The Pain, Enjoyment and General Active scale measures pain intensity, enjoyment of life and general activity each on a 0 - 10 with higher scores indicating worse pain impact. The score is the average of all items.
Time Frame
Change in PEG from baseline to 6 weeks
Title
Aim #3 Opioid Dose on Timeline followback
Description
Patient reported opioid dose on the timeline followback
Time Frame
Change in opioid dose from baseline to 12 weeks
Title
Aim 3: PEG (Pain, Enjoyment, General Activity)
Description
The Pain, Enjoyment and General Active scale measures pain intensity, enjoyment of life and general activity each on a 0 - 10 with higher scores indicating worse pain impact. The score is the average of all items.
Time Frame
Change in PEG from baseline to 12 weeks.
Secondary Outcome Measure Information:
Title
Aim #1 Qualitative Interviews
Description
Semi-structured qualitative interviews will be conducted with patients and physical therapists after they review a mindfulness treatment protocol. Analysis will generate qualitative themes that will be used to modify the treatment protocol in preparation for Aim #2.
Time Frame
1 month
Title
Aim #2: Physical therapist retention (competency assessment)
Description
Percent of physical therapists who attend the competency assessment.
Time Frame
3 months
Title
Aim #2: Randomized physical therapists
Description
Percentage of physical therapists invited who consent to be randomized
Time Frame
6 months
Title
Aim #2: Physical therapist enrollment
Description
Percent of physical therapists presented the study who choose to enroll in the study
Time Frame
2 months
Title
Aim #3 Patient Reported: Patient Reported Outcomes Measurement Information System (PROMIS) Physical Function Short Form 6b (PROMIS-6b)
Description
Reported as a T-Score with a mean of 50 and a SD of 10
Time Frame
Change from baseline to 6 weeks and change from baseline to 12 weeks
Title
Aim #3 Patient Reported:Patient Reported Outcomes Measurement Information System (PROMIS)PROMIS Sleep Disturbance Short Form 6a
Description
Reported as a T-Score with a mean = 50 and a SD = 10
Time Frame
Change from baseline to 6 weeks and change from baseline to 12 weeks
Title
Aim #3 Patient Reported: Pain Catastrophizing Scale short form
Description
Scores range 0- 24. Higher scores mean greater catastrophizing.
Time Frame
change from baseline to 6 weeks and change from baseline to 12 weeks
Title
Aim #3 Patient Reported: Patient Health Questionnaire-2 (PHQ-2)
Description
Scores range from 0-6. Higher scores mean greater likelihood of depression
Time Frame
Changes on the Patient Health Questionnaire-2 (PHQ-2) questions from baseline to 6 weeks and from baseline to 12 weeks.
Title
Aim #3 Patient Reported: Generalized Anxiety Disorder-2 (GAD-2)
Description
2 items summed range 0 - 6. Higher score mean greater likelihood of anxiety
Time Frame
Changes on the Generalized Anxiety Disorder-2 (GAD-2) questions from baseline to 6 weeks and baseline to 12 weeks.
Title
Aim #3 Patient Reported: Patient Global Impression Scale-Change
Description
Scores range from 0 - 7 with higher score equating to greater improvement in condition
Time Frame
Changes on the Patient Global Impression Scale-Change questions from baseline to 6 weeks and from baseline to 12 weeks.
Title
Aim #3 Patient Reported: Pain Self-Efficacy Questionnaire
Description
Scores range from0 - 60 with higher scores indicating greater levels of confidence in dealing with pain
Time Frame
changes from baseline to 6 weeks and from baseline to 12 weeks
Title
Aim #3 Patient Reported: Mindfulness-Five Facet Mindfulness Questionnaire (FFMQ)
Description
15 items scores range from 15 - 75 higher scores indicate greater mindfulness
Time Frame
Change from baseline to 6 weeks and baseline to 12 weeks
Title
Aim #3 Patient Reported: Positive Reappraisal Subscale of Cognitive Emotion Regulation Questionnaire
Description
4 items each scored 1 - 5. Higher the score the more positive reappraisal.
Time Frame
change from baseline to 6 weeks and change from baseline to 12 weeks
Title
Aim #3 Patient Reported: Savoring Beliefs Inventory
Description
24 items. Composite scores are obtained by averaging the subscales after rescoring the negatively worded items. Higher scores equate to greater savoring.
Time Frame
Changes from baseline to 6 weeks and change from baseline to 12 weeks
Title
Aim #3 Patient Reported: Participant-report health care utilization measures
Description
Measure health care use (imaging, physician visits, medications)
Time Frame
12 weeks
Title
Aim #3 Patient Reported: Short Assessment of Patient Satisfaction
Description
7 items. Each item scored 0 - 4 . Reverse score items 1, 3, 5 and 7. Sum scores. Range from 0 (extremely dissatisfied to 7 (extremely satisfied)
Time Frame
12 weeks
Title
Aim #3 Patient Reported: The Internal Pain Activity Questionnaire (IPAQ) short form measures physical activity
Description
7 items. Measures metabolic equivalents (METS). Higher score in METS equates to greater activity.
Time Frame
Baseline
Title
Aim #3 Reach: Patients offered and enrolled
Description
The percentage of patients with chronic muscle pain and long-term opioid treatment offered participation who choose to enroll.
Time Frame
3 months
Title
Aim #3 Reach: Physical therapists with enrolled patients
Description
The percentage of physical therapists who have a patient enrolled on their schedule
Time Frame
3 months
Title
Aim #3 Effectiveness: REDCap Outcomes Collected
Description
The percentage of outcomes collection using REDCap
Time Frame
3 months
Title
Aim #3 Effectiveness: Timeline Follow Back
Description
Percentage of Timeline Followback collected
Time Frame
3 months
Title
Aim #3 Adoption: Qualitative interviews
Description
Semi-structured qualitative interviews will be conducted with patient, PT, support staff interviews regarding their lived experience integrating mindfulness and physical therapy. Analysis will generate qualitative themes that will be used to plan for a fully-powered trial.
Time Frame
3 months
Title
Aim #3 Adoption: Mindfulness Oriented Recovery Enhancement component (MORE)
Description
Percentage of patients enrolled after I-EPT training that report receiving any MORE component.
Time Frame
3 months
Title
Aim #3 Implementation: Fidelity
Description
Mindfulness Oriented Recovery Enhancement _functional measure (Modified MORE-FM) fidelity measure during patient encounters. 21-item scale - total scores range from 0 - 114. Scores are summed and averaged.
Time Frame
3 months
Title
Aim #3 Implementation: Qualitative Interviews
Description
Semi-structured qualitative interviews will be conducted with patient, PT, support staff interviews regarding their lived experience integrating mindfulness and physical therapy. Analysis will generate qualitative themes that will be used to plan for a fully-powered trial.
Time Frame
3 months
Title
Aim #3 Implementation: Percentage of patients managed by PT
Description
The percentage of patients managed by a single trained physical therapist (don't cross over between physical therapists)
Time Frame
3 months
Title
Aim #3: Maintenance: Qualitative Interviews
Description
Semi-structured qualitative interviews will be conducted with patient, PT, support staff interviews regarding their lived experience integrating mindfulness and physical therapy. Analysis will generate qualitative themes that will be used to plan for a fully-powered trial. These interviews will be used to understand potential barriers for future implementation of physical therapy integrated with mindfulness
Time Frame
3 months
Title
Aim #3: Physical therapist retention
Description
The percentage of physical therapists who participate in the fidelity assessments
Time Frame
3 months
Title
Aim #3: Patient retention
Description
Percentage of patients managed by study physical therapists who are retained at baseline, 6- and 12-week follow-up.
Time Frame
baseline, 6 weeks, 12 weeks
Title
Aim #3: Screened patients
Description
Percentage of patients screened who are eligible
Time Frame
6 months
Title
Sleep duration
Description
hours and minutes of actual sleep during past month
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Aim 1 Physical Therapist Inclusion Criteria: Employed at least .5 (Full Time Equivalent) Manages patients with musculoskeletal conditions Exclusion Criteria: None Aim 2 and 3 Physical Therapist Inclusion Criteria: Employed at least .5 (Full Time Equivalent) Manages patients with musculoskeletal conditions Physical Therapist Exclusion Criteria: -Attended any experiential (i.e., practice sessions with real or simulated patients) mindfulness training to be used for patient care Attended any patient care specific mindfulness training lasting more than 3 hours. Self-report using mindfulness interventions such as savoring and cognitive reappraisal (core components of MORE) as a primary intervention strategy for the majority of their caseload for patients with chronic musculoskeletal pain. Aims 1, 2 and 3 Patient Inclusion Criteria: Age 18-75 English Speaking Diagnosis of musculoskeletal pain condition involving the spine and/or peripheral joint(s) Current musculoskeletal pain present for greater than or equal to 3 months. Use of prescription opioids for most of the last 90 days (self-report) Patient Exclusion Criteria: Currently pregnant Currently receiving mind-body treatment for musculoskeletal pain from a healthcare provider (e.g. PT, chiropractic, massage therapy, etc) Currently receiving treatment for substance use disorder Musculoskeletal pain condition related to a fracture or surgical procedure in the past 6 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jake Magel, PhD
Phone
801-581-4709
Email
jake.magel@hsc.utah.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Priscilla Blosser, RN
Phone
801-213-6117
Email
priscilla.blosser@hsc.utah.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jake Magel, PhD
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jason Beneciuk, PhD
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jake Magel
First Name & Middle Initial & Last Name & Degree
Priscilla Blosser

12. IPD Sharing Statement

Learn more about this trial

Physical Therapy Integrated With Mindfulness for Patients With Chronic Pain and Opioid Treatment

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