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  2. Patient recruitment - Wikipedia

    en.wikipedia.org/wiki/Patient_recruitment

    Patient recruitment is the process of finding and enrolling suitable participants for clinical trials. It is a crucial aspect of drug development and medical research, as it affects the validity, reliability, and generalizability of the results.

  3. Snowball sampling - Wikipedia

    en.wikipedia.org/wiki/Snowball_sampling

    Snowball sampling is a recruitment method that employs research into participants' social networks to access specific populations. According to research mentioned in the paper written by Kath Browne, [20] using social networks to research is accessible. In this research, Kath Browne used social networks to research non-heterosexual women.

  4. Research participant - Wikipedia

    en.wikipedia.org/wiki/Research_participant

    A research participant, also called a human subject or an experiment, trial, or study participant or subject, is a person who voluntarily participates in human subject research after giving informed consent to be the subject of the research. A research participant is different from individuals who are not able to give informed consent, such as ...

  5. Research site - Wikipedia

    en.wikipedia.org/wiki/Research_site

    In a network of research sites where all are recruiting study participants, sites with low recruitment benefit from coaching from sites with high recruitment. [1] Characteristics of good clinical research sites include setting good timelines, early participant recruitment, and having a management plan for efficiency. [2]

  6. Clinical equipoise - Wikipedia

    en.wikipedia.org/wiki/Clinical_equipoise

    The condition of the patient is also a factor in these risks. Ensuring that trials meet the standards of clinical equipoise is an important part of patient recruitment in this regard; it is likely that past trials that did not meet conditions of clinical equipoise suffered from poor recruitment. [6]

  7. Patient and public involvement - Wikipedia

    en.wikipedia.org/wiki/Patient_and_Public_Involvement

    Designing research. Public members help designing the research to make sure it is feasible, ethical and relevant. This happens usually before applying for funding. Managing research. Public involvement in the steering group or managing committee that oversees the research. Undertaking research. Members of the public help carrying out the research.

  8. Justice (research) - Wikipedia

    en.wikipedia.org/wiki/Justice_(research)

    In research ethics, justice regards fairness in the distribution of burdens and benefits of research. For example, justice is a consideration in recruiting volunteer research participants, in considering any existing burdens the groups from which they are recruited face (such as historic marginalisation) and the risks of the research, alongside the potential benefits of the research.

  9. Multiple baseline design - Wikipedia

    en.wikipedia.org/wiki/Multiple_Baseline_Design

    Nonconcurrent multiple baseline studies apply treatment to several individuals at delayed intervals. This has the advantage of greater flexibility in recruitment of participants and testing location. For this reason, perhaps, nonconcurrent multiple baseline experiments are recommended for research in an educational setting. [3]