Recruitment methods and yield rates for a multisite clinical trial exploring risk reduction for Alzheimer's disease (rrAD)

Author:

Szabo‐Reed Amanda N.12,Hall Tristyn3,Vidoni Eric D.14,Van Sciver Angela1,Sewell Monica5,Burns Jeffrey M.14,Cullum C. Munro67,Gahan William P.8,Hynan Linda S.69,Kerwin Diana R.1011,Rossetti Heidi6,Stowe Ann M.11,Vongpatanasin Wanpen8,Zhu David C.12,Zhang Rong37,Keller Jeffrey N.8,Binder Ellen F.5

Affiliation:

1. KU Alzheimer's Disease Research Center, University of Kansas Medical Center Fairway Kansas USA

2. Department of Internal Medicine University of Kansas Medical Center Kansas City Kansas USA

3. Institute for Exercise and Environmental Medicine Texas Health Presbyterian Hospital Dallas Dallas USA

4. Department of Neurology University of Kansas Medical Center Kansas City Kansas USA

5. Department of Internal Medicine Division of Geriatrics & Nutritional Science Washington University School of Medicine in St. Louis St. Louis Missouri USA

6. Department of Psychiatry UT Southwestern Medical Center Dallas Texas USA

7. Department of Neurology UT Southwestern Medical Center Dallas Texas USA

8. Institute for Dementia Research and Prevention Pennington Biomedical Research Center Baton Rouge Louisiana USA

9. Peter O'Donnell Jr. School of Public Health UT Southwestern Medical Center Dallas Texas USA

10. Kerwin Research Center and Memory Care Dallas Texas USA

11. Department of Neurology University of Kentucky Lexington Kentucky USA

12. Department for Radiology Michigan State University East Lansing Michigan USA

Abstract

AbstractINTRODUCTIONThe risk reduction for Alzheimer's disease (rrAD) trial was a multisite clinical trial to assess exercise and intensive vascular pharmacological treatment on cognitive function in community‐dwelling older adults at increased risk for Alzheimer's disease.METHODSEligibility, consent, and randomization rates across different referral sources were compared. Informal interviews conducted with each site's project team were conducted upon study completion.RESULTSInitially, 3290 individuals were screened, of whom 28% were eligible to consent, 805 consented to participate (87.2% of those eligible), and 513 (36.3% of those consented) were randomized. Emails sent from study site listservs/databases yielded the highest amount (20.9%) of screened individuals. Professional referrals from physicians yielded the greatest percentage of consented individuals (57.1%). Referrals from non‐professional contacts (ie, friends, family; 75%) and mail/phone contact from a site (73.8%) had the highest yield of randomization.DISCUSSIONProfessional referrals or email from listservs/registries were most effective for enrolling participants. The greatest yield of eligible/randomized participants came from non‐professional and mail/phone contacts. Future trials should consider special efforts targeting these recruitment approaches.Highlights Clinical trial recruitment is commonly cited as a significant barrier to advancing our understanding of cognitive health interventions. The most cited referral source was email, followed by interviews/editorials on the radio, television, local newspapers, newsletters, or magazine articles. The referral method that brought in the largest number of contacts was email but did not result in the greatest yield of consents or eligible participants. The sources that yielded the greatest likelihood of consent were professional referrals (ie, physician), social media, and mail/phone contact from study site. The greatest yield of eligible/randomized participants came from non‐professional contacts and mail/phone contact from a site. Findings suggest that sites may need to focus on more selective referral sources, such as using contact mailing and phone lists, rather than more widely viewed recruitment sources, such as social media or TV/radio advertisements.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

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