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Mindfulness Based Intervention for Depression
Study Summary
This trial will study how different aspects of mood disorders can be improved with integrative health treatments.
- Depression
- Stress
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
What is the maximum capacity of participants in this medical research project?
"Confirmed. Data from clinicaltrials.gov suggests that this medical trial, which was first published on October 26th 2021, is in the recruitment phase and still searching for 75 participants to be enrolled at 1 site."
What qualifications are necessary to be eligible for this research endeavor?
"This trial is searching for 75 persons of ages 18 to 65 who are suffering from depression. In addition, additional qualifications include: the ability to comprehend English enough for providing informed consent and completing questionnaires; an IDS score of at least 18; remitted or currently depressed patients (as determined by PHQ-9 scores); a lack of cold/flu symptoms on day of collection, no infections within two weeks prior to collection, and no known sickle cell disease; at most 550mLs donated in blood donation activities in the past 8 weeks with not more than one draw per week; stable maintenance antidepressant/anti-anxiety medications over"
Is this research project currently accepting participants?
"Affirmative. According to the data on clinicaltrials.gov, the trial which was initially posted October 26th 2021 is actively recruiting patient volunteers. 75 participants are required from a sole medical centre for this study's completion."
Does the study protocol permit applicants aged 70 or older?
"This medical study is open to adults aged 18 to 65, while there are 218 and 1070 trials available for minors and seniors respectively."
Who else is applying?
What state do they live in?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
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