A Randomized Trial of Recruitment Strategies for Research Participation

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University of Pennsylvania

Status

Completed

Conditions

This Study Will Focus on Recruitment Strategies and Attitudes Towards Research Among Patients Considering Participation in 2 Parent Randomized Controlled Trials
Cancer
Research Ethics

Treatments

Behavioral: High-level recruitment strategy consent form
Behavioral: Mid-level recruitment strategy consent form

Study type

Interventional

Funder types

Other

Identifiers

NCT02697799
823491

Details and patient eligibility

About

In a multicenter, randomized clinical trial of attitudes towards research participation, we will evaluate the ethics, effectiveness, and cost- effectiveness of three recruitment strategies for research participation in a mobility trial among hospitalized patients and a smoking cessation trial among patients with depression.

Enrollment

1,296 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Eligible for parent RCT
  2. 18 years or older
  3. No prior knowledge of recruitment strategies used for this trial
  4. Speaks English

Exclusion criteria

1)Prior knowledge of recruitment strategies used for this trial

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

1,296 participants in 3 patient groups

High-level recruitment strategy
Experimental group
Description:
Subjects in this group will receive pre-consent messaging and a consent form with a high-level recruitment strategy for research participation in the parent study. The consent form will provide information on the first page, under the header that describes the purpose of the study, as well as in the consent sections describing the cost to participate in the study.
Treatment:
Behavioral: High-level recruitment strategy consent form
Mid-level recruitment strategy
Experimental group
Description:
Subjects in this group will receive pre-consent messaging and a consent form with a mid-level recruitment strategy for research participation in the parent study. The consent form will provide information on the first page, under the header that describes the purpose of the study, as well as in the consent sections describing the cost to participate in the study.
Treatment:
Behavioral: Mid-level recruitment strategy consent form
No modified recruitment strategy
No Intervention group
Description:
Subjects in this group will receive consent form without a modified recruitment strategy for research participation in the parent study.

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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