Clinical Research Directory

The Effect of Mindfulness-Based Stress Reduction Program

This randomized controlled study evaluate the effect of the Mindfulness-Based Stress Reduction Program on the state-trait anxiety, hopelessness, self-compassion and care burden of the families of psychotic patients. The hypothesis of this study is that the Mindfulness-Based Stress Reduction Program improves the state-trait anxiety, hopelessness, self-compassion and care burden of the families of psychotic patients.

Workplace Stress Among School Teachers: Minfulness Based Stress Reduction Intervention

This randomized controlled trial aims to evaluate the effectiveness of an eightweek Mindfulness-Based Stress Reduction (MBSR) program in reducing workplace stress among secondary school teachers from public and private schools in the Malakand Division, Khyber Pakhtunkhwa, Pakistan. Eligible teachers experiencing moderate to high workplace stress will be randomly assigned to either an MBSR intervention group or a wait-list control group. Stress levels will be assessed before and after the intervention using the Workplace Stress Scale (WSS) and the Perceived Stress Scale (PSS). The study also aims to compare stress levels between public and private school teachers and investigate gender differences in intervention outcomes. This description aligns with your synopsis objectives and design.

A Reinforced Mindfulness-Based Intervention to Reduce Problematic Drinking Among Hispanic Emerging Adults

This study is a trial to evaluate a mindfulness program designed for Hispanic young adults. Participants will be randomly assigned to one of two groups: (1) an in-person, 8-week mindfulness program (one 1.5-hour session per week at FIU's MMC campus), or (2) an assessment-only control group. Regardless of group assignment. Participants will be asked to complete online surveys at baseline, after an 8-week period, and again one month later. They will also be asked to provide a fingerpick blood sample and have their heart rate and blood pressure measured at four timepoints: baseline, 1 month, 2 months, and 3 months after baseline. Participation will involve up to 16 hours over approximately 14 weeks. This includes time for completing baseline assessments, participating in the 8-week intervention (if assigned), and completing post-program and follow-up assessments. There are no serious risks of participating in this study, but some of the questions during the assessments, interview, or the fingerpick may cause you discomfort. The main benefit from participating in this clinical trial is that participants may experience personal benefits from learning mindfulness techniques.