Testing the Pain Relief of musculOskeletal Conditions and Arthritis Using Culturally Tailored InterVentions for Black Elders (PROACTIVE) Intervention: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Chronic musculoskeletal pain (CMP), while a leading cause of physical disablement, is a neglected national health disparity issue in Black communities. The purpose of this study is to test a novel culturally congruent pain self-management intervention. A total of 120 persons aged 50-92, self-identifying as Black or African American having CMP will be invited to participate in this study. The primary outcome measured throughout this 3-year study is movement-evoked pain (MEP).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 92
Healthy Volunteers: f
View:

• Self-identify as being part of the Black American diaspora (Black/African American, Afro-Caribbean)

• Age 50-92 years

• 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)

• 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)

• 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

• 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.)

• Able to read, write, and understand English at sixth-grade level

Locations
United States
Florida
University of Florida
RECRUITING
Gainesville
Contact Information
Primary
Staja Q Booker, PhD, RN
bookers@ufl.edu
352-273-6351
Backup
Fern Webb, PhD
fern.webb@jax.ufl.edu
904-244-9859
Time Frame
Start Date: 2025-05-07
Estimated Completion Date: 2027-10-01
Participants
Target number of participants: 120
Treatments
No_intervention: Usual Care (Control Group)
The control group will continue their usual pain treatment and self-management (SM) routines.~Participations will not receive in-depth culturally congruent education, prayer skills, or financial counseling. Usual care is expected to vary between participants.
Experimental: PROACTIVE
This is a four-session pain self-management (SM) intervention designed to reduce movement-evoked pain by providing participants with behavioral support that addresses social determinants of health: (1) culturally congruent SM education + SM resource toolkit, (3) active prayer support, and (3) financial counseling.
Sponsors
Collaborators: National Institute of Nursing Research (NINR)
Leads: University of Florida

This content was sourced from clinicaltrials.gov