Instructions for Developing an Informed Consent Document General Information. Describe the purpose(s) of this research study in lay terms. Purpose of the Study. Procedures. Risks. Benefits. Compensation, Costs and Reimbursement. Withdrawal or Termination from Study. Confidentiality.
Illinois law permits minors age 12 and older to receive a limited amount of counseling services or psychotherapy on an outpatient basis without parental consent, and providers are prohibited from notifying the minor's parents without the minor's consent “unless the facility director believes such disclosure is ...
In an intact family, the general rule is that either parent may consent to the child's treatment. Typically a therapist or counselor may want to get the consent of the other parent, or may want to inform the other parent of the treatment, but at other times, such action may not be possible or warranted.
In general, one or both parents or a guardian must be provided with the information ordinarily required for informed consent, so that they may decide whether to allow the child to participate, and children capable of assent must also express their willingness to participate.
They are held to standards of care. This is especially true in the case of providing counseling treatment for minor children. Professional counselors need to obtain from both parents, consent for the child's treatment.
At a minimum, a well-designed informed consent form will address the following information: Risks and benefits of treatment. Fees and payment policies. Confidentiality and its limits. Contact information and communication. Social media policy and general boundaries. Emergency procedures.
Under Illinois law, anyone under the age of 18 is considered a minor. A minor often needs parental or guardian consent for most healthcare services. However, you can access some services on your own. Exceptions to when you can consent for yourself depends on your legal status, medical condition or treatment.
Informed Consent for Psychology Research Purpose: Inform the participants about the purpose of the research, the anticipated duration of the study, and the procedures that will be used. Right to withdraw: Tell participants that they have the right to decline to participate in the study.