Depression and Anxiety Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who report pain of more than 3 out of 10 that has lasted longer than 3 months and stops them from doing at least one activity they would like to do
- People who live independently in the community (not in a care facility)
- People who live in the Central Maryland area
- People who score 5 or higher on a standard depression questionnaire (called the PHQ-9) on at least two separate occasions over a two-week period
- People who are considered "pre-frail" (meeting one or two markers of physical frailty) or "frail" (meeting three or more markers of physical frailty), as measured by a standard frailty assessment (confirm with trial site)
- People who have at least one limitation with either basic daily activities (such as bathing or dressing) or more complex daily tasks (such as managing finances or using transportation)
Who may not be able to join:
- People who have been hospitalised more than 3 times in the past year
- People who are currently receiving physical therapy
- People who have been given a terminal diagnosis with an expected survival of less than one year
- People with more than moderate intellectual or cognitive impairment, as measured by a standard short mental status questionnaire (confirm with trial site for specific scoring details)
- People who are not able to speak or understand English
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Janiece L Taylor, PhD, Johns Hopkins School of Nursing
Phone: 443-287-4503
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in Pain Intensity as assessed by the Patient Reported Outcomes Measurement Information System (PROMIS); Change in Pain Interference as assessed by the PROMIS Pain Interference; Change in Depressive Symptoms as assessed by the Patient Health Questionnaire 9 (PHQ-9); Change in Depressive Symptoms as assessed by the PROMIS 57
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.