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Clinical Trials/NCT01442285
NCT01442285
Completed
Not Applicable

The Mental Health and Dynamic Referral for Oncology Protocol (MHADRO)

University of Massachusetts, Worcester1 site in 1 country1,000 target enrollmentApril 2011
ConditionsCancerDistress

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University of Massachusetts, Worcester
Enrollment
1000
Locations
1
Primary Endpoint
Decrease in psychological stress
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to understand more about meeting the psychosocial needs of people who have cancer.

Detailed Description

The investigators are interested in the feasibility of using computer assisted screening and assessment to meet the psychosocial needs of people with cancer. The investigators are studying two different interventions. Both groups will receive health information, referral information, and resources. One group will also receive tailored feedback reports.

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
April 2015
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Massachusetts, Worcester
Responsible Party
Principal Investigator
Principal Investigator

Edwin Boudreaux

Study Principle Investigator

University of Massachusetts, Worcester

Eligibility Criteria

Inclusion Criteria

  • cancer diagnosis

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Decrease in psychological stress

Time Frame: 12 months

Both groups will receive a full assessment, referral information, and resources. Only the intervention group will have the option of immediately sending their contact information to a counselor/mental health provider and receive a tailored feedback report with specific recommendations about managing their psychological and social needs, and provide education about ways to improve their quality of life. We anticipate that distressed subjects assigned to the Intervention Group will exhibit larger decreases in psychological distress when compared against the Control Group.

Secondary Outcomes

  • Reduced distress(12 months)

Study Sites (1)

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