Description of the Lived Experiences of Family Caregivers for People With Mental Health Comorbidities
NCT07760701
Anxiety, Anxiety Disorders
Lusaka, Lusaka Province, Zambia
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.
Looking for future studies?
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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.
Published trials that share one or more normalized conditions with this study.
NCT07760701
Anxiety, Anxiety Disorders
Lusaka, Lusaka Province, Zambia
View Trial DetailsNCT06993662
Anxiety, Anxiety Disorders
Athens, Greece
View Trial DetailsNCT07741422
Anxiety, Anxiety Disorders
Guangzhou, Guangdong, China
View Trial DetailsNCT06942637
Adolescents, Anxiety
Bandung, West Java, Indonesia
View Trial Details