Mindfulness-based Cognitive Therapy for the Chronic Pain-depression Co-morbidity Among Older Blac… (NCT07336342) | Clinical Trial Compass
CompletedNot Applicable
Mindfulness-based Cognitive Therapy for the Chronic Pain-depression Co-morbidity Among Older Black Adults in the Community; The Quiet Focus Open Pilot
United States12 participantsStarted 2024-11-15
Plain-language summary
The goal of this clinical trial is to pilot an adaptation of mindfulness-based cognitive therapy for chronic pain and depression. The main questions it aims to answer in a later fully powered randomized controlled trial are:
* Is an adaptation of mindfulness-based cognitive therapy for older Black adults able to improve quality of life?
* Will an adapted mindfulness based cognitive therapy reduce pain interference to a greater degree than a traditional health enhancement program?
Who can participate
Age range
50 Years – 120 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Older adult (age ≥ 50)
. All individuals who identify with one or more nationalities or ethnic groups originating in any of the Black racial groups of Africa
. Pain in muscles, joints, bones, or associated soft tissues (NRS\>4) lasting longer than 3 months
. Depressed (PHQ-9 score of 5-14)
. English fluency/literacy
. Ability and willingness to participate via in-person and video
. No change to type or dose of antidepressant medications for at least 6 weeks prior to screening
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The Credibility and Expectancy Questionnaire
Timeframe: From enrollment to 3 months from the end of treatment at 8 weeks
2
The Client Satisfaction Questionnaire
Timeframe: Administered at the end of treatment at 8 weeks and at the three month follow up visit.
3
Modified Patient Global Impression of Change
Timeframe: At end of 8 week program (post test) and again at 3 month follow up visit.