Sponsor: National Cancer Institute
Sponsor Study ID: R01CA281740
Study Title: Improving Proactive Approaches for Cancer Survivors' Mental Health Treatment
CTO #: 104095
NCT Number: NCT06582784
Phase: N/A
Protocol Type: Supportive Care
Age Group: Adults
Disease Sites: Unknown Sites
Study Objectives: To examine the effectiveness of proactive ID + DMHI compared with proactive ID + UC on depression symptom severity among ILLIC with depression as measured by the change in the PHQ-9 score from baseline. To examine the effectiveness of proactive ID + DMHI compared with proactive ID + UC on anxiety and quality of life among ILLIC with depression as determined by the (1) change in the Hospital Anxiety and Depression Scale, Anxiety subscale score from baseline and (2) change in the Functional Assessment of Cancer Therapy-General score from baseline.