Clinical Trials Logo

Clinical Trial Summary

The goal of this project is to test the effectiveness, feasibility and acceptability of a common elements intervention delivered by community mental health workers for adults with a history of adverse childhood experiences. "Common elements" interventions build cognitive, emotional, interpersonal, and behavioral skills to help address trauma-related distress and build resilience. This will be accomplished using a randomized control trial with Apache adults ages 25-65 with recent suicidal behaviors, self-injurious behaviors, and/or binge substance use.


Clinical Trial Description

This is a mixed-methods study with qualitative data informing adaptation and evaluation of a common elements intervention delivered by community mental health specialists, named "My Pathway to Healing." Apache partners selected a randomized control trial, as it is a rigorous study design for understanding whether an intervention works, to evaluate the effectiveness of the My Pathway to Healing intervention delivered by community mental health specialists (CMHS). This intervention integrates psychoeducation, relaxation techniques, problem solving and cognitive coping, and addresses safety (when identified as a problem area). The intervention used in the intervention arm of our study has been developed for the specific context and culture of White Mountain Apache. Those randomized into the My Pathway to Healing group will receive 4-8 hour-long sessions with a community mental health specialist, taking place over 8-12 weeks. The exact number of sessions will depend on presentation and symptom level using a stepped care approach where participants receive only what they need, but the provider can provide additional sessions if needed (i.e., increased element dosage; additional optional elements for specific issues). Those randomized into the control will continue to receive the standard case management via the Apache surveillance system. These control participants will be offered the My Pathway to Healing Program upon completion of the study. Participants will be asked to partake in 5 study assessments. For intervention participants these assessments will take place at: baseline, after their last intervention session (endline; approximately 8-12 weeks post-baseline) and 4, 8, and 12 weeks post-endline. For control participants, these assessments will take place at: baseline, 8-12 weeks post-baseline (the maximum time the intervention would last; will be referred to as an endline) and 4, 8 and 12 weeks post-endline. These assessment visits will be conducted by Research Program Assistants. Assessments will take approximately 45-90 minutes to complete. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04585906
Study type Interventional
Source Johns Hopkins Bloomberg School of Public Health
Contact
Status Active, not recruiting
Phase N/A
Start date July 19, 2022
Completion date August 2025

See also
  Status Clinical Trial Phase
Completed NCT04105725 - Balanced Lifestyle for Undergraduate Excellence - Mobile (Project BLUEM) N/A
Recruiting NCT05491551 - Alcohol-ROC-Training N/A
Completed NCT02064998 - Two Consecutive Randomized Controlled Trials Using Mobile Phone Applications for Risky Alcohol Use N/A
Completed NCT02336204 - Alcohol Consumption Relation With Nutritional Knowledge and Body Weight N/A
Recruiting NCT05565989 - Alcohol Consumption, Intention Implementation and Mindfulness Meditation (ADUC-Volet 3 " Prevention ") N/A
Completed NCT01125371 - Computerized Brief Alcohol Intervention (BI) for Binge Drinking HIV At-Risk and Infected Women N/A
Recruiting NCT06084832 - Smartphone Application for University Students With Binge Drinking Behavior N/A
Completed NCT04853628 - An Animation- Versus Text-based Computer-tailored Game Intervention to Prevent Alcohol Consumption in Adolescents N/A
Completed NCT03449095 - Understanding Alcohol Reward in Social Context N/A
Recruiting NCT05522075 - Reducing Blood Pressure in Mid-life Adult Binge Drinkers N/A
Not yet recruiting NCT06215664 - Game-Based Intervention to Reduce Alcohol Use Among Sexual and Gender Minority Youth N/A
Completed NCT03652675 - Understanding and Intervening With Heavy Drinking Among Patients With HIV and HCV N/A
Completed NCT03288896 - Alerta Alcohol. Web-based Computer-tailored Intervention for Binge-drinking Prevention in Spanish Adolescents N/A
Completed NCT02842073 - An Open Label Trial of Bupropion and Naltrexone for Binge Drinking Phase 2
Active, not recruiting NCT03567434 - Alcohol and Neural Cardiovascular Control in Binge Drinkers N/A
Not yet recruiting NCT06326099 - Brief Binge Eating and Drinking Online Intervention N/A
Recruiting NCT03224416 - Individual and Contextual Factors That Influence Sexual Decisions N/A
Active, not recruiting NCT05882214 - Metabolic Changes Induced by NMN in Healthy Subjects With Acute Binge Drink N/A
Completed NCT01546025 - Brief Alcohol Intervention for School-to-Work Transitions N/A
Completed NCT01503255 - A Stage 2 Cognitive-behavioral Trial: Reduce Alcohol First in Kenya Intervention Phase 1