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Control condition for Cancer

N/A
Recruiting
Led By Qian Lu, MD, PHD
Research Sponsored by M.D. Anderson Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up time frame: through study completion; an average of 1 year
Awards & highlights

Study Summary

"This trial aims to understand the experiences of Asian American immigrant breast cancer survivors and how writing about their experiences may impact their health."

Who is the study for?
This trial is for Asian American breast cancer survivors who have immigrated to the United States. It's designed to understand their experiences and how writing about these experiences can impact their health.Check my eligibility
What is being tested?
Participants will be asked to complete questionnaires and write essays as a form of therapy. The study aims to evaluate if this writing therapy can provide health benefits for cancer survivors.See study design
What are the potential side effects?
Since the intervention involves writing, there are no direct physical side effects expected from participating in this trial.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~time frame: through study completion; an average of 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and time frame: through study completion; an average of 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Measure: Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

Trial Design

2Treatment groups
Experimental Treatment
Group I: Intervention ConditionExperimental Treatment2 Interventions
Participants will be asked to write about different topics regarding their cancer experience. During session 1, participants will be asked to write about the stress of having cancer and their strategies for coping with stressors associated with their cancer (i.e., stress and coping). During session 2, participants will be asked to write about their deepest feelings regarding their cancer experience (i.e., emotional disclosure). During session 3 and the booster session (at 9-month follow-up), participants will be asked to write about positive thoughts and feelings regarding their experience with cancer.
Group II: Control conditionExperimental Treatment2 Interventions
Participants will be asked to write about facts regarding their cancer diagnosis and treatment in writing sessions.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Questionnaires
2013
Completed Phase 2
~3330

Find a Location

Who is running the clinical trial?

M.D. Anderson Cancer CenterLead Sponsor
2,997 Previous Clinical Trials
1,792,674 Total Patients Enrolled
Qian Lu, MD, PHDPrincipal InvestigatorM.D. Anderson Cancer Center
~128 spots leftby Aug 2026
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