- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04554576
Escoge Salud (Choose Health): a Chronic Pain Self-Management Program in Middle to Older Age Hispanic Americans
Escoge Salud (Choose Health) Effects and Sustainability of a Chronic Pain Self-Management Program in Middle to Older Age Hispanic Americans
Study Overview
Status
Conditions
Detailed Description
Managing chronic pain in the US costs approximately $635 billion and half of this expenditure is for joint and arthritis related pain syndromes. Interestingly, compared with non-Hispanic whites (NHWs), Hispanic Americans (HAs) report significantly lower rates of chronic pain with consistently higher levels of pain intensity in both population and clinically based studies. Chronic musculoskeletal pain (CMP) incidence increases with age and the HA aging population is among the fastest growing segments of the US population. Despite reporting more intense pain, HA are less likely to seek medical care versus NHWs for acute and chronic pain. Lack of access, cultural stoicism and an external locust of control are thought to explain why HAs seek care at a reduced rate. Psychological factors play a significant role in pain experience, HAs may employ catastrophic thinking and experience more pain related anxiety which are predictors of exacerbated pain experience. Pain comorbidities may be amenable to treatment with appropriate, culturally sensitive treatment focusing on enhancing self-efficacy to manage the complex array of psychological pain comorbidities. There is a societal impact of undertreating chronic pain in the HA population. While HAs have the lowest rate of short-term sick usage (<1-2 days), they have the highest rate of long-term sick usage (>31 days). This increased long-term time off puts HAs at risk of losing their job if the time off exceeds Family Leave and Medical Act minimums. Lastly, it is well documented, HAs are hesitant to take strong pain medication and there is conflicting evidence surrounding taking over-the-counter medications for pain management. There is a need to provide culturally sensitive, effective chronic pain management treatments for HAs.
There have been 5 well designed studies (n=931) demonstrating efficacy of a trans-created Spanish version of the Chronic Disease Self-Management Program (CDSMP) for HAs with chronic musculoskeletal pain. CDSMP has demonstrated effectiveness in improving pain intensity, self-efficacy (SE) and health behaviors in a community setting . The intervention is a healthcare provider and/or peer led 2.5 hour self-management training session, 1 time per week for 6 weeks taught in a group setting in Spanish. The program is grounded in Bandura's Social Cognitive Theory and uses goal setting and problem solving as corner stones to create a personalized self-management program. Improvements post-intervention in SE predict sustainability of health behaviors and maintenance of improved health status in the long term. Additionally, remote non-frequent health care provider feedback has been associated with maintenance of health behaviors, however this his not been tested in the HA population.
The purpose of this study is to test the feasibility (patient satisfaction and change in health status) after bringing the CDSMP programming to a large urban hospital based medical center that does not currently offer a culturally sensitive, self-management training program in Spanish middle to older age HAs with chronic pain. The secondary aim is to pilot the effectiveness of an every 6th week phone/video visit feedback visit for 24 months on both health status and healthcare utilization.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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San Francisco, California, United States, 94118
- KaiserPermanente
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Spanish Speaking
- Had 1 or 2 outpatient dispense records of NSAIDS between Jan 1 2018 to Dec 31 2018.
- 5 doctor office visits between 07/01/2017 - 12/31/2018 for any health program.
- Non-malignant musculoskeletal pain for at least 6 months
- Interested in learning self-management
- Ability to have telephone/video visit every 6 weeks
- Ability to travel to medical center 1x/week for 6 weeks in the afternoon for 2.5 hours
Exclusion Criteria:
- Major psychiatric or substance abuse problem
- Mild cognitive impairment/dementia
- Malignant pain or terminal illness
- Listed in the Non-contact database
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: 6-week self-management and remote feedback for 6 months
All participants will receive the 6-week self-management program and after, half the group will be randomized to an every 6th week healthcare provider feedback phone or video visit session for 6 months (4 visits over 24 months).
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The CDSMP meets for 2.5 hours for 6 weeks. Topics covered are: understanding pain, finding resources, mindfulness, pain science, pacing, exercise, relaxation, communication, sex/intimacy, healthy eating, weight and medication management, making treatment decisions and confronting fears. Participants are encouraged to create their own personal health goals and make weekly action plans to meet their personal goals. Each week participants learn new tools and problem-solving techniques to meet their health goals and themes are repeated throughout 6-week period to ensure understanding and integration. Participants are encouraged to problem-solve and ask questions to the group about creating and carrying out their self-management plan. The intervention follows the content of the book Programa de Manejo Personal del Dolor Crónico (Living a Healthy Life with Chronic pain)
Other Names:
After the 6-week self management program, half the participants will be randomized to an every 6 weeks for 6 months phone or video visit from a health care provider, in Spanish.
The phone or video sessions will include: review previous action-plans (goals) and provide support in forming new action-plans (goals)
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ACTIVE_COMPARATOR: 6-week self-management and control group for 6 months
All participants will receive the 6-week self-management program and after, half will be randomized to a 6 month control grup
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The CDSMP meets for 2.5 hours for 6 weeks. Topics covered are: understanding pain, finding resources, mindfulness, pain science, pacing, exercise, relaxation, communication, sex/intimacy, healthy eating, weight and medication management, making treatment decisions and confronting fears. Participants are encouraged to create their own personal health goals and make weekly action plans to meet their personal goals. Each week participants learn new tools and problem-solving techniques to meet their health goals and themes are repeated throughout 6-week period to ensure understanding and integration. Participants are encouraged to problem-solve and ask questions to the group about creating and carrying out their self-management plan. The intervention follows the content of the book Programa de Manejo Personal del Dolor Crónico (Living a Healthy Life with Chronic pain)
Other Names:
After the 6-week self-management program, half the participants will be randomized to a control group for 6 months.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Self Efficacy
Time Frame: baseline to 6-weeks
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Spanish Arthritis self-efficacy scale (ASES).
This tool has 8 questions rating 'certainty' in ability to manage health and chronic pain.
It is scored on a visual analogue scale from 1-10, 1= very uncertain to 10= very certain.
Higher scores indicate more self-efficacy.
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baseline to 6-weeks
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Patient Reported Outcome Measurement Information System (PROMIS) Global Health
Time Frame: baseline to 6-weeks
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Spanish PROMIS Global Health v1.2 measures global physical, mental and social health.
It has 10 questions, 9 of which are answered on a 5-point Likert scale and 1 question on a visual analogue scale where 0=no pain and 10=worst pain imaginable.
PROMIS measures are scored on a t-score metric where 50 is set to be the population norm and higher scores indicate better global health.
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baseline to 6-weeks
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Pain Catastrophizing
Time Frame: baseline to 6-weeks
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Spanish Pain Catastrophizing Scale (PCS) evaluates 3 distinct phenomenon which are characterized by feelings of helplessness, active rumination and excessive magnification associated with pain experience.
The questionnaire has 13 questions and is scored on a 5-point Likert scale, 0= not at all to 4 = all the time.
Higher scores indicate more catastrophizing.
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baseline to 6-weeks
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Health Distress
Time Frame: baseline to 6-weeks
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Health Distress Scale evaluates distress and worry due to illness.
It has 4 question that are answered on a 5-point Likert scale where 0= none of the time and 5= all of the time.
Higher scores indicate more distress and worry.
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baseline to 6-weeks
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Patient Satisfaction
Time Frame: baseline to 6-weeks
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Adapted from Camino con Gusto study.
3 questions on satisfaction with the intervention scored on scored on a 4-point scale: 1 = Strongly disagree, 2 = Disagree, 3 = Agree, 4 = Strongly agree.
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baseline to 6-weeks
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Patient Global Impression
Time Frame: baseline to 6-weeks
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Patient Global Impression of Change (PGIC) captures the patients satisfaction with the intervention by asking "How satisfied or dissatisfied are you with the self-management program?' and is scored on a 7-point scale where 7-point scale where -3 =very dissatisfied 0= neither satisfied or dissatisfied and 3= very satisfied.
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baseline to 6-weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Doctors office visits
Time Frame: 6 weeks to 30-34 weeks
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Number of Primary Care doctors office visits
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6 weeks to 30-34 weeks
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Emergency Room use
Time Frame: 6 weeks to 30-34 weeks
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Number of Emergency Room visits
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6 weeks to 30-34 weeks
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Self Efficacy
Time Frame: 6-weeks to 30-34 weeks
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Spanish Arthritis self-efficacy scale (ASES).
This tool has 8 questions rating 'certainty' in ability to manage health and chronic pain.
It is scored on a visual analogue scale from 1-10, 1= very uncertain to 10= very certain.
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6-weeks to 30-34 weeks
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PROMIS Global Health
Time Frame: 6-weeks to 30-34 weeks
|
Spanish PROMIS Global Health v1.2 measures global physical, mental and social health.
It has 10 questions, 9 of which are answered on a 5-point Likert scale and 1 question on a visual analogue scale where 0=no pain and 10=worst pain imaginable.
|
6-weeks to 30-34 weeks
|
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Pain Catastrophizing
Time Frame: 6-weeks to 30-34 weeks
|
Spanish Pain Catastrophizing Scale (PCS) evaluates 3 distinct phenomenon which are characterized by feelings of helplessness, active rumination and excessive magnification associated with pain experience.
The questionnaire has 13 questions and is scored on a 5-point Likert scale, 0= not at all to 4 = all the time
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6-weeks to 30-34 weeks
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Health Distress
Time Frame: 6-weeks to 30-34 weeks
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Health Distress Scale evaluates distress and worry due to illness.
It has 4 question that are answered on a 5-point Likert scale where 0= none of the time and 5= all of the time
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6-weeks to 30-34 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amy Gladin, DPT, senior physical therapist
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1326143-3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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