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Study participation includes a baseline enrollment visit consisting of informed consent, completion of self-report inventories, short-term recording of blood pressure and heart rate, and a HIRREM assessment.
Consultations covered explanations of the risk and appropriate screening programme and, after informed consent, completion of a national questionnaire to capture data on risk factors for secondary cancers after HL treatment.
The exclusion criteria for participation in the extension study were: participation in another clinical trial involving respiratory intervention, or new diagnosis of psychiatric disorder which in the judgment of the investigator could interfere with provision of informed consent, completion of tests, therapy, or follow-up.
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As participation involved responding to an anonymised electronic survey which included participant information, informed consent was inferred by completion.
Interested individuals will then be referred to a fieldworker, who will request informed consent for the completion of a brief screener for assessing whether or not they meet the eligibility criteria listed above.
Participants who provided informed consent to complete the travel questionnaire were given the questionnaire for self-completion in the study centre.
All participants were provided with an information sheet to explain the study and informed consent was assumed on completion and submission of the survey responses.
The participant gave written and informed consent before enrollment or completion of any study-specific procedures.
The participant or their representative gave written and informed consent before enrolment or completion of any study-specific procedures.
All participants gave informed consent and received $30 upon completion of each interview.
We obtained informed consent from cancer clinicians for the completion of the online survey.
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