Mindfulness-Based Interventions Targeting First-Generation College Student Retention in Rural Environments
NCT06789731
Anxiety, Anxiety Disorders
Sioux Falls, South Dakota, United States
View Trial DetailsNCT Number: NCT01909921
The purpose of this study is to assess the effectiveness of a Relaxation Response Intervention for Depression offered to low income populations at Massachusetts General Hospital (MGH) - Chelsea, Revere and Charlestown health centers.
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Notify Me21 year and older
All sexes
Observational
This is a retrospective review of medical records. The study aims to evaluate the effects of participation in the Relaxation Response Intervention for Depression Clinical groups, on patient measures of: 1) depression, anxiety and perceived stress; 2) work productivity and activity impairment; 3) demand for, and adherence to behavioral medicine; 4) medication use for depression and/or anxiety; and 5) dose-response effects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
-
Time frame: Pre- and Post-Intervention (8 weeks)
Time frame: Pre- and Post- Intervention (8 weeks)
Time frame: Pre- and Post-Intervention (8 weeks)
Massachusetts General Hospital
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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