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Tundra lists 3 Psychosocial Distress clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.
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NCT07673731
Addressing Cancer-Related Distress Through Survivorship Care in Community Oncology
The goal of this study is to understand whether providing a structured survivorship care visit at the beginning of cancer treatment is associated with changes in distress and quality of life in adults with cancer receiving treatment in a community oncology clinic. The main questions it aims to answer are: * Is participation in a structured survivorship visit at the start of active treatment associated with changes in psychological distress? * Is participation in the survivorship visit associated with changes in quality of life? Participants will: * Be asked to complete questionnaires about their level of distress and overall quality of life. * Participate in a single survivorship visit with the clinic's Physician Assistant at the Ellis Medical Oncology Clinic. * Complete the same questionnaires again approximately two weeks and one month after the survivorship visit.
Gender: All
Ages: 18 Years - Any
Updated: 2026-06-29
1 state
NCT07583069
Psychosocial Effects of a Trauma-Informed Artificial Intelligence-Supported Chatbot in Adults Newly Diagnosed With Cancer
The goal of this clinical trial is to evaluate whether a trauma-informed, artificial intelligence-supported chatbot can reduce psychological distress and unmet psychosocial needs in adults newly diagnosed with cancer.: * Does the chatbot reduce trauma-related distress and anxiety levels compared to standard care? * Does the chatbot decrease unmet psychosocial needs in patients following a new cancer diagnosis? Researchers will compare the chatbot intervention to standard care to determine whether the chatbot provides additional psychosocial benefit. Participants will: * Be randomly assigned to either the chatbot intervention group or the standard care group * Use the chatbot freely for 12 weeks (intervention group only) * Complete questionnaires at baseline, 1 month, and 3 months * Be monitored for any psychological risk indicators during the study period
Gender: All
Ages: 18 Years - Any
Updated: 2026-05-13
NCT04269005
SomPsyNet - Prevention of Psychosocial Distress Consequences in Somatic Medicine: a Model for Collaborative Care
This study is to evaluate the impact of the "stepped and collaborative care model" (SCCM) on health-related quality of life in somatic hospital patients with psychosocial distress.
Gender: All
Ages: 18 Years - Any
Updated: 2023-09-21