Intervention group for Symptom Management

Stephenson Cancer Center, Oklahoma City, OK
Symptom Management+1 More ConditionsIntervention group - Behavioral
18 - 99
All Sexes
What conditions do you have?

Study Summary

This trial will assess the feasibility of using a smartphone app to help manage anxiety and depression for cancer patients receiving radiation treatments.

Eligible Conditions
  • Symptom Management
  • Treatment Non-Adherence

Treatment Effectiveness

Study Objectives

1 Primary · 0 Secondary · Reporting Duration: 8 weeks

8 weeks

Trial Safety

Awards & Highlights

No Placebo Group
All patients enrolled in this trial will receive the new treatment.

Trial Design

1 Treatment Group

Intervention group
1 of 1

Experimental Treatment

60 Total Participants · 1 Treatment Group

Primary Treatment: Intervention group · No Placebo Group · N/A

Intervention group
Experimental Group · 1 Intervention: Intervention group · Intervention Types: Behavioral
First Studied
Drug Approval Stage
How many patients have taken this drug
Intervention group

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: 8 weeks

Who is running the clinical trial?

University of OklahomaLead Sponsor
434 Previous Clinical Trials
99,423 Total Patients Enrolled

Eligibility Criteria

Age 18 - 99 · All Participants · 2 Total Inclusion Criteria

Mark “Yes” if the following statements are true for you:
You have been diagnosed with breast, gynecological or head and neck cancer.
You live in the community, not in a hospital or institution.