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Spots Global Cancer Trial Database for Using Effective Provider-Patient Communication to Improve Cancer Screening Among Low Literacy Patients

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Trial Identification

Brief Title: Using Effective Provider-Patient Communication to Improve Cancer Screening Among Low Literacy Patients

Official Title: Using Effective Provider-Patient Communication to Improve Cancer Screening Among Low Literacy Patients

Study ID: NCT01361035

Study Description

Brief Summary: What's the purpose of this study? This 4-year study is designed: (1) to teach primary care physicians how to recognize low health literacy patients and effectively counsel them on cancer screening using risk communication and shared decision making and (2) to assess the impact of training on changes in physician communication behavior and changes in low health literacy patients' cancer screening behaviors. This study proposal is based on the hypothesis that physician training in cancer screening guidelines, health literacy, and communication skills will improve provider-patient interactions during encounters dealing with preventive health maintenance especially cancer screening. How will the proposed study be implemented? Thirty-two physicians in the New Orleans metropolitan area will be recruited and randomly assigned to one of two groups. The unit of randomization will be the health care organization or clinic. The intervention group will receive training in health literacy, cancer screening, risk communication and shared decision-making. The control group will not receive communication training until the end of the study. Physicians in both groups will undergo three clinic visits with standardized patients (actors trained to portray real patients; mystery shoppers) but they will not be aware that they are conducting visits with actors. The visits will occur at study enrollment and at 6 and 12 months. At the end of each clinic visit, the standardized patients will rate the physicians' communication skills. Each physician assigned to the intervention group will receive verbal feedback on communication skills from the standardized patients and complete a web-based tutorial. Physicians in the control group will not have access to the web-based tutorial until the end of the study. For each physician, 10-15 patients with limited health literacy will be recruited to the study. Each patient will rate his/her perceived involvement with care and global satisfaction with care at study enrollment and annually for three years. Age and gender-appropriate referral rates for breast, cervical and colorectal cancer screening and patients' receipt of such screening will be assessed annually for three years. All study physicians, regardless of group assignment, will receive performance feedback (report cards) on their cancer screening rates among low health literacy patients in their clinic.

Detailed Description:

Eligibility

Minimum Age: 40 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Tulane Communty Health Center at Covenant House, New Orleans, Louisiana, United States

Tulane Faculty Practice, New Orleans, Louisiana, United States

EXCELth - Ida Hymel Community Health Center, New Orleans, Louisiana, United States

DCSNO St Cecelia Medical Center, New Orleans, Louisiana, United States

DCSNO Carrollton Medical Center, New Orleans, Louisiana, United States

Contact Details

Name: Eboni Price-Haywood, MD, MPH

Affiliation: Tulane University School of Medicine

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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