The PROACTIVE Study for Black Elders

NCT ID
NCT06512727
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
University of Florida
Conditions
Chronic Pain, Movement Evoked Pain, Musculoskeletal Pain, Osteoarthritis, Pain, Chronic

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: Testing the Pain Relief of musculOskeletal Conditions and Arthritis Using Carefully Tailored InterVEntions (PROACTIVE) Intervention: A Randomized Controlled Trial

Enrollment: 120 participants (Estimated).

What is being studied

  • Behavioral: PROACTIVE Intervention

Who may be eligible

Ages
50 Years to 92 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Self-identify as being part of the Black American diaspora (Black/African American, Afro-Caribbean) 2. Age 50-92 years 3. Self-report chronic musculoskeletal pain (CMP) as defined as persistent or recurrent pain lasting 6 months or longer that arises as part of a disease or injurious process directly affecting bone(s), joint(s), muscle(s), or related soft tissue(s) 4. Self-report a chronic musculoskeletal condition (e.g., osteoarthritis, chronic low back pain) in at least one lower extremity joint (hip, knee, low back, or ankle pain) 5. Report chronic musculoskeletal symptoms: aching, stiffness, or swelling in a major lower extremity joint or low back on most days (4-5/7) of the week 6. Have (or be eligible for) a healthcare insurance plan in the state of Florida (Medicare, Medicaid, Medicare Advantage plans, Blue Cross/Blue Shield, Humana, Aetna, etc.) 7. Able to read, write, and understand English at sixth-grade level Exclusion Criteria: 1. Unwilling to be randomized to either study arm 2. Self-reported diagnosis of sickle cell disease or related thalassemias 3. History of major neurological event (e.g., stroke) or current neurological disease (e.g., Parkinson's disease, multiple sclerosis, epilepsy) 4. Major cardiovascular problem in the past 6 months that would cause shortness of breath and/or chest pain (e.g. myocardial infarction, coronary artery bypass graft, or valve replacement, pulmonary embolism or deep venous thrombosis) or uncontrolled Hypertension (Systolic Blood Pressure (SBP) \> 170 mmHg, Diastolic Blood Pressure (DBP) \> 90 mmHg) OR Hypotension (SBP \<90 mmHg, DBP \<60 mmHg) 5. Currently undergoing curative or palliative chemotherapy or radiation for active cancer 6. Severe physical impairment (e.g., a major activity of daily living disability requiring use of wheelchair as primary method of mobility, or unable to dress, bath, use the toilet, or transfer independently) 7. Serious mental health disorder requiring hospitalization within past 12 months 8. Severe sensory deficit (severe hearing loss or blindness)

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: United States

  • Florida, United States: 1

Sample of listed locations

  • University of Florida — Gainesville, Florida, 32610, United States — Recruiting

Study details

Start date
May 7, 2025
Primary completion date
August 1, 2027
Completion date
October 1, 2027
First posted
July 22, 2024
Collaborators
National Institute of Nursing Research (NINR)

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT06512727
Registry last updated
June 4, 2026
QualifiedStudies registry data refreshed
October 2, 2026
QualifiedStudies record fetched
October 2, 2026

View NCT06512727 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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