University of Texas Health Science Center School of Public Health
Houston, Texas, 77030, United States
NCT Number: NCT01911208
The purpose of this study is to test a recruitment intervention to increase racial and ethnic diversity in clinical trials. The trial will be conducted in specialty care clinics. In RECRUIT minorities are those underrepresented in clinical trials and include:
* African Americans/ Blacks * Asians * Native Hawaiians/Other Pacific Islanders * Hispanic/Latinos * Native Americans/Alaskan Natives
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Notify Me18 year–85 year
All sexes
Interventional
Not applicable
Houston, Texas, 77030, United States
Low minority participation in clinical trials limits our ability to assess and address potential differences in therapeutic responses. To address the problem of low minority recruitment we are initiating a randomized trial of a recruitment intervention (RECRUIT) funded by the National Institute on Minority Health and Health disparities (NIMHD) to increase racial/ethnic diversity in clinical trials.
Our specific approach is directed toward multi-site trials conducted at specialty clinics within academic centers with recruiting venues that include community practices or practices of colleagues in other areas of the academic center. The intervention will focus on approximately 60 specialty clinics. Clinical sites will be randomized to the intervention or control group. The target of the intervention will be the site investigators and clinical trial coordinators.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion:
A parent trial must :
The clinical site must
Exclusion criteria
Sites randomized to RECRUIT are taught skills to develop a tailored recruitment intervention encompassing continuous quality improvement and patient navigation.
Non-intervention control.
Time frame: Up to 2 years
Minorities as defined in this trial include those underrepresented in clinical trials and considered underrepresented by NIH criteria with the addition of those of Asian descent.
Time frame: up to 2 years
Differences between intervention and control sites in number of participant referrals.
Time frame: up to 2 years
Numbers and types of activities reported on recruitment logs by all sites.
Time frame: up to 2 years
Change from baseline in physician investigator and coordinator outcome expectations (intervention sites only).
Time frame: up to 2 years
Qualitative key informant phone interviews of the physician investigators and coordinators (intervention and control sites).
Time frame: up to 2 years
Potential/enrolled participant satisfaction with intervention and control trial site investigators and coordinators. Subjects will be given a satisfaction survey at screening and at every follow up visit.
Time frame: up to 2 years
Change from baseline in physician investigator and coordinator self-efficacy(intervention sites only).
The University of Texas Health Science Center, Houston
Other
Acronym: RECRUIT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.