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Study details
Enrolling now

Engage Psychosocial Intervention for Cancer Symptoms

Duke University
NCT IDNCT06555588ClinicalTrials.gov data as of Apr 2026
Target enrollment

190

Study length

about 3.5 years

Ages

18+

Locations

1 site in NC

What this study is about

This trial is testing a new psychosocial symptom management intervention called ENGAGE for people with advanced breast, prostate, lung, or colorectal cancer. Participants will be randomly assigned to receive ENGAGE or standard supportive care. Patient-reported outcomes will be measured at the beginning of the trial, after 2 months, and after 4 months.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Participate in ENGAGE
  • 2.Participate in Supportive Care

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: MD Anderson Symptom Inventory (MDASI) Interference with Daily Living Scale

Secondary: Brief Fatigue Inventory (BFI), Brief Pain Inventory (BPI), MD Anderson Symptom Inventory (MDASI) Interference with Daily Living Scale, MD Anderson Symptom Inventory (MDASI) Symptom Severity Scale, Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety-Short Form, Patient-Reported Outcomes Measurement Information System (PROMIS) Depression-Short Form, Patient-Reported Outcomes Measurement Information System (PROMIS) Self-Efficacy for Managing Symptoms

Body systems

Gastroenterology, Oncology