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Doctor of Missiology - Biola University

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Cook School <strong>of</strong> Intercultural Studies<br />

Department <strong>of</strong> Intercultural Studies: <strong>Doctor</strong> <strong>of</strong> <strong>Missiology</strong><br />

PHRRC SECTION 5.11<br />

1. A disclosure <strong>of</strong> appropriate alternative procedures or courses <strong>of</strong> treatment, if any, which might<br />

be advantageous to the participant.<br />

2. Anticipated circumstances under which the participant's participation may be terminated by the<br />

investigator without regard to the participant's consent.<br />

3. Any additional costs to the participant that may result from participation in the research.<br />

4. The consequences <strong>of</strong> a participant's decision to withdraw from the research and procedures for<br />

orderly termination <strong>of</strong> participation by the participant.<br />

5. Details regarding authorization for access to the participant's personal records (school,<br />

university, hospital, employment or others).<br />

6. Details regarding any recording <strong>of</strong> their voices or images for data collection unless the research<br />

consists solely <strong>of</strong> naturalistic observations in public places, and it is not anticipated that the<br />

recording will be used in a manner that could cause personal identification or harm.<br />

7. The amounts and terms <strong>of</strong> any proposed payments or other form <strong>of</strong> remuneration to<br />

participants.<br />

8. When experimental treatments are used, clarify to participants at the outset <strong>of</strong> the research (1)<br />

the experimental nature <strong>of</strong> the treatment; (2) the services that will or will not be available to the<br />

control group(s) if appropriate; (3) the means by which assignment to treatment and control<br />

groups will be made; (4) available treatment alternatives if an individual does not wish to<br />

participate in the research or wishes to withdraw once a study has begun; and (5) compensation<br />

for or monetary costs <strong>of</strong> participating including, if appropriate, whether reimbursement from<br />

the participant or a third-party payer will be sought.<br />

Guideline #4: Waiver <strong>of</strong> Written Informed Consent<br />

A waiver <strong>of</strong> the requirements for informed consent is granted only where research would not<br />

reasonably be assumed to create distress or harm and involves:<br />

1. The study <strong>of</strong> normal educational practices, curricula or classroom management methods<br />

conducted in educational settings<br />

2. Only anonymous questionnaires, naturalistic observations or archival research for which<br />

disclosure <strong>of</strong> responses would not place participants at risk or criminal or civil liability or damage<br />

their financial standing, employability or reputation and confidentiality is protected.<br />

Date: March 2004 Page 7 <strong>of</strong> 13

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