Improving Proactive Approaches for Cancer Survivors' Mental Health Treatment

Sponsor:

National Cancer Institute

Sponsor Study ID:

R01CA281740

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.

eConsent:

Not available

Study Documents:

Open Study Documents
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