Purpose

The aim of this research study is to test the feasibility of a physical and mental health intervention (Positive Minds, Strong Joints or PMSJ) for Black adults with knee osteoarthritis (OA).

Condition

Eligibility

Eligible Ages
Over 50 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age≥50 - BMI ≤ 40 kg/m2 - Self-identify as Black (including African American) - Knee pain ≥4/10 on a 11 numeric scale over the past week - Scored 5 or more on either the Patient Health Questionnaire (PHQ-9) and/or the Generalized Anxiety Disorder 7-item Scale (GAD-7) - Can speak and understand English at a sufficient level to understand the study procedures and informed consent - Available for study duration - Available to attend in-person intervention sessions at the community location - Able to attend remote sessions

Exclusion Criteria

  • Knee, hip or ankle replacement - Intra-articular corticosteroid or hyaluronic acid knee injection within 3 months - Knee surgery within past 6 months - Currently receiving or received within 3-months any PT for knee OA - Currently receiving or received within 3 months any mental health intervention (excluding pharmacologic treatments) - Planning to initiate physical therapy for joint or low back pain in the next 3months - Planning to initiate any mental health treatment (excluding pharmacologic treatments) in the next 1 month. - Systemic inflammatory arthritis (e.g., rheumatoid arthritis) - Neurologic conditions (e.g., stroke, Parkinson's disease, etc.) - Contraindications to starting an exercise program. - Suspected substance abuse - Lack capacity to consent - Pregnancy (self-report) - Participation in another clinical trial for any joint or muscle pain - Planning for a major surgery in the next 6 months - Having high risk mental health symptoms (active suicidality, bipolar disorder, mania, psychosis, schizophrenia) - Receiving chemotherapy or radiation therapy for cancer (except non-melanoma skin cancer)

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Positive Minds Strong Joints
Participants will receive an individual mental health intervention through a zoom video-call once a week for 10 weeks and a community-based group exercise intervention once a week for 10 weeks.
  • Behavioral: Positive Minds, Strong Joints
    In this10-week physical and mental health intervention, participants will receive recommended exercise intervention and evidence-based mental health intervention for pain, depression and anxiety.

Recruiting Locations

Boston University
Boston, Massachusetts 02215

More Details

Status
Recruiting
Sponsor
Boston University Charles River Campus

Study Contact

Deepak Kumar, PhD,PT
617-358-3037
kumard@bu.edu

Detailed Description

In this feasibility study, at least 20 and up to 40 Black Adults will be enrolled to receive PMSJ intervention. Participants who will take part in this research study will be in it for about 26 weeks. Participants will receive a one-hour individual session of psychoeducation, mindfulness, and cognitive behavior therapy skills for 10 weeks via a HIPAA-protected zoom video-call or over the telephone. In addition, they will receive a community-based group exercise and pain education program once a week for 10 weeks. Participants will also continue to receive their usual care. Participants will be asked to take surveys at five time points (i.e.) before the start of the 10-week intervention (baseline visit), mid-way through the intervention (week 5), end of the 10-week intervention (post-intervention), 6 weeks after the intervention (week 16) and 12 weeks after the intervention (week 22). Brief surveys will also be completed weekly throughout the study. The surveys will be about pain, function, quality of life, mood, social support, sleep, etc. At baseline and post-intervention visits, all participants will also be asked to wear a small movement sensor on their lower back for 7 days of continuous movement and physical activity monitoring. During both of these 7-day periods, participants will complete a single remote assessment of their walking. Feasibility of the intervention will be determined post-intervention by outcome measures such as recruitment rate, retention rate, and adherence.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.