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Spots Global Cancer Trial Database for Web-Based Tailored Educational Program in Improving Nurse Communication With Patients About Clinical Trials

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Trial Identification

Brief Title: Web-Based Tailored Educational Program in Improving Nurse Communication With Patients About Clinical Trials

Official Title: Oncology Nurse IMPACT: Improving Communication With Patients About Clinical Trials

Study ID: NCT02129517

Study Description

Brief Summary: This pilot, randomized clinical trial studies a web-based tailored educational program in improving nurse communication with patients about clinical trial treatment options. A web-based tailored educational program may empower and prepare nurses to discuss clinical trial treatment options with patients and may also increase patient participation in clinical trials.

Detailed Description: PRIMARY OBJECTIVES: I. To develop and pilot test a theory-driven, web-based, tailored, interactive educational program (Oncology Nurse IMPACT: Improving Communication with Patients about Clinical Trials) for oncology nurses to address barriers to discussing clinical trials with patients. II. To implement Oncology Nurse IMPACT on a national level and conduct a formal program evaluation. III. To evaluate the mediators and moderators of education program effect on intentions to discuss clinical trials with patients. OUTLINE: Participants are assigned to 1 of 2 intervention arms. ARM I: Oncology nurses watch web-based informational video clips addressing knowledge, attitudes, subjective norms, and perceived behavioral control (barriers of discussing clinical trials with patients). They also watch role-play video clips to help improve perceived behavioral control and address attitudinal barriers. ARM II: Oncology nurses view online clinical trials educational materials developed based upon National Cancer Institute (NCI) clinical trials educational materials for health care providers. The educational materials contain text and tables as presented on the NCI Website. After completion of study intervention, participants are followed for 3 months.

Keywords

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center, Cleveland, Ohio, United States

Contact Details

Name: Neal Meropol, MD

Affiliation: Case Comprehensive Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Name: Barbara Daly, PhD

Affiliation: Case Comprehensive Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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