Skip to content

MOTIVATE to Improve Outcomes for Older Veterans With Musculoskeletal Pain and Depression

CompletedNot applicableNCT05220202
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The proposed study seeks to evaluate effectiveness, implementation processes, and cost of MOTIVATE among older Veterans with chronic musculoskeletal (MSK) pain and comorbid depressive symptoms.

Study details

Official title
MOTIVATE to Improve Outcomes for Older Veterans With Musculoskeletal Pain and Depression
Interventions
  • Behavioral: Behavioral Intervention Group (MOTIVATE)
Sponsor
VA Office of Research and Development
Collaborators
Dallas VA Medical Center; Michael E. DeBakey VA Medical Center
Start date
2023-09-20
Primary completion
2026-07-09
Sex
All
Age range
from 60 Years to 99 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
2

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * English- speaking * Self-reported musculoskeletal (MSK) pain (include Chronic low back pain (cLBP) +/- radiating symptoms, osteoarthritis (OA), fibromyalgia) on most days for the past 3 months that interferes with daily activities * Pain intensity that is 4+/10 on the numerical pain rating scale * Pain interference threshold 5+ on 3-item Pain, Enjoyment of Life, and General Activity scale (PEG-3) * Depressive symptoms, 10+ on the Patient Health Questionnaire-9 (PHQ-9) * Capable of participating in home-based activity * Interested in participating in a non-pharmacologic program Exclusion Criteria: * No telephone * Not English speaking * Unwilling to be randomized to either study arm * Not interested in participating in a non-pharmacologic program * Self-reported uncorrected hearing and visual impairments precluding ability to participate in telephone sessions or read pedometer screen * Significant (moderate or severe) cognitive impairment (3+ errors) on six-item screening exam * Self-reported dependence on wheelchair, bed-bound, or severe balance impairment or severe osteoarthritis (OA)\* (resulting in inability to participate in physical activity intervention) * Illness requiring hospitalization within the last 3 months that interferes with a home-based physical activity intervention (e.g., fall, gout attack, stroke, heart attack, heart failure, surgery for blocked arteries) * Suicidal intent (see suicide screening protocol), uncontrolled psychotic disorder or psychiatric hospitalization within 1 year, or enrolled in active substance use program (confirmed with scripted protocol over telephone)

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05220202