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INFORMED CONSENT FOR EXERCISE PROGRAM Explanation of the Exercise Program: All exercise sessions will be designed based on the client\'s individual needs and supervised by trainers). The sessions
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Informed consent is a process through which a patient or participant voluntarily confirms their willingness to participate in a particular intervention or study after being informed of all relevant details, risks, and benefits. Shared decision-making involves collaboration between the healthcare provider and the patient, ensuring that treatment decisions reflect the patient's values and preferences.
Typically, healthcare providers, researchers conducting clinical trials, and institutions conducting medical or psychological assessments are required to obtain and file informed consent from patients or study participants.
To fill out informed consent, providers should present clear and understandable information about the purpose of the intervention or study, the procedures involved, potential risks, benefits, and alternatives. Participants should sign the document to indicate their understanding and agreement.
The purpose of informed consent is to ensure that individuals are fully aware of what participation entails, thus protecting their autonomy and rights. Shared decision-making aims to involve patients in their own care, enhancing satisfaction and adherence to treatment.
Informed consent documents should include details such as the purpose of the study, potential risks and benefits, confidentiality measures, the right to withdraw at any time, and contact information for questions or concerns.
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