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Compassion clinical trials

View clinical trials related to Compassion.

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NCT ID: NCT06289426 Recruiting - Depression Clinical Trials

Online Yoga for Improving the Well-being of Desk-based Workers

Start date: February 15, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to evaluate the effectiveness of an 8-week online yoga intervention in improving the well-being and productivity of desk-based workers. The main questions it aims to answer are: - How effective is an 8-week online yoga intervention in improving the well-being (mental and physical) and productivity (work engagement and job performance) of the yoga group compared with passive controls? - Are there any differences in well-being and work-related measures between the yoga and control groups? Participants in the yoga group will practice yoga three days a week for 8 weeks and will be compared with a wait-listed control group, which will continue with the usual routine for 8 weeks. Researchers will evaluate the impact of yoga on the well-being and productivity of desk-based workers.

NCT ID: NCT06251869 Recruiting - Compassion Clinical Trials

Electrocoagulation vs. Cold Knife Cutting in Joint Arthroplasty (Electrocoagulation vs Scalpel)

evs
Start date: March 15, 2024
Phase:
Study type: Observational

Comparison of clinical outcomes of electrocoagulation and non-electrocoagulation techniques in total hip and knee arthroplasty surgery

NCT ID: NCT05949060 Recruiting - Stress Reaction Clinical Trials

Effects of Self-Compassion Practice on Stress Reactivity Among Sexual Minority Women

Start date: July 17, 2023
Phase: N/A
Study type: Interventional

This project will test the ability of brief self-compassion training to attenuate physiological and subjective responses to induced stress among sexual minority women, transgender people, and nonbinary people.

NCT ID: NCT05791825 Recruiting - Health, Subjective Clinical Trials

Evaluation of the CHIME Intervention for Improving Early Head Start/Head Start Educator Well-being

CHIME
Start date: March 13, 2023
Phase: N/A
Study type: Interventional

This study will test how well a mindfulness-based intervention called CHIME improves the emotional well-being of educators in Early Head Start and Head Start (EHS/HS) settings. The study also will examine if there are any benefits to young children's social emotional health as a result of the CHIME program. Researchers will compare educators who participate in CHIME to educators who are asked to participate at a later time to see if there are benefits to their emotional health and teaching practices.

NCT ID: NCT04700878 Recruiting - Clinical trials for Psychological Stress

A Randomized Controlled Evaluation of a Compassion-course for Healthcare Professionals

ICOP
Start date: February 1, 2021
Phase: N/A
Study type: Interventional

The aim is to investigate whether an internet-based compassion course of five modules contributes to reducing stress of conscience and work-related stress, increase the experience of professional quality of life and self-compassion in healthcare professionals.

NCT ID: NCT03305952 Recruiting - Compassion Clinical Trials

Cognitively-Based Compassion Training for Breast Cancer Survivors

CBCT-BC
Start date: January 11, 2016
Phase: N/A
Study type: Interventional

There is a growing number of evidence of how mindfulness training enhances psychological and physical well-being and coping strategies in patients with oncological illnesses. However, there are very few studies analyzing the efficacy of Compassion-Based Interventions on breast cancer survivors. The goal of this study is to analyze enrollment, participant satisfaction and adherence to program and differences in psychological well-being, health related quality of life, fear of illness recurrence, compassion and self-compassion variables after a Compassion-Based Intervention in a Spanish breast cancer survivor sample. This study is a randomized clinical trial of a secularized intervention called Cognitively-Based Compassion Training (CBCT). Subjects (n = 58) were randomly assigned to CBCT (n = 28) or a treatment as usual control group (TAU) (n = 28). Participants in the CBCT intervention condition were asked to meet weekly for a two (2) hour long session during two months. Pre-post-intervention and six month follow-up measures took place to evaluate: psychological well-being (somatic, depressive, and anxious symptomatology), health related quality of life (physical, social, emotional, and functional); psychological stress, coping strategies and triggering cognitions linked to cancer recurrence fear, self-compassion, compassion and mindfulness and awareness in both intervention and wait list groups. CBCT is a promising and potentially useful intervention to enhance physical and emotional well-being in breast cancer survivors. Nevertheless, future randomized trials are needed and a process of cultural adaptation required.