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Treatment as Usual clinical trials

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NCT ID: NCT05954585 Recruiting - Treatment as Usual Clinical Trials

Family Navigator Intervention

Start date: December 2, 2023
Phase: N/A
Study type: Interventional

This study will develop and examine the feasibility and acceptability of a family navigator protocol while leveraging digital health communication. It will employ an ecological model within a socio-cultural theoretic framework of mental health service disparities and barriers to treatment.

NCT ID: NCT05948631 Recruiting - Treatment as Usual Clinical Trials

MISC-IPV: A Community-Based Intervention for Children Traumatized by Intimate Partner Violence

MISC-IPV
Start date: February 14, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

This study adapts and evaluates preliminary outcomes of the Mediational Intervention for Sensitizing Caregivers (MISC) for women and children of color who have survived domestic violence.

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.