{"database":"ecrin-mdr-crc","file_versions":[],"scores":null,"additional":{"omics_type":["Clinical"],"study_start_year":["2018"],"data_sharing_plan":["What data will be shared? Anonymized raw data \tWhen will data be available (start and end dates)? Upon publication of manuscript and for 5 years from that date. \tAvailable to whom? Available to researchers who request \tAvailable for what types of analyses? Raw data available for secondary analysis or other reasonable uses determined by the PI. \tBy what mechanism will data be made available? Upon request to authors by email to PI: usha.gurunathan@health.qld.gov.au"],"condition":["Colorectal Cancer","Cancer-Bowel-Back passage (rectum) or large bowel (colon)","Postoperative Complications","Anaesthesiology-Other anaesthesiology"],"disease":["Colorectal Cancer","Cancer-bowel-back Passage (rectum) Or Large Bowel (colon)","Anaesthesiology-other Anaesthesiology","Postoperative Complications"],"study_type":["Observational"],"full_dataset_link":["https://newmdr.ecrin.org/Study/2467472"],"location":["Australia"],"study_start_month":["9"],"repository":["ECRIN MDR"],"study_status":["Completed"],"additional_accession":[]},"is_claimable":false,"name":"A preliminary survey on the baseline characteristics and preferences for a multimodal prehabilitation in patients scheduled for elective colorectal cancer resection","description":"Interventions: Patients scheduled for bowel resection for colorectal cancer will be recruited. They will be asked to complete questionnaires about their health conditions, fitness levels, psychological status,nutritional status and preferences for a proposed prehabilitation programme assisted by the cancer care co-ordinator. This would require approximately an hour of their time.\nThat would be the end of their participation in the research project. They will not be required to participate in any programme as a part of this project.\nPrimary outcome(s): To investigate patient preferences for a proposed future prehabilitation program for colorectal cancer patients\nInstrument: Semi-strucured interview[Time of baseline interview..]\nStudy Design: Purpose: Screening;Duration: Cross-sectional;Selection: Defined population;Timing: Prospective","dates":{"creation":"2018-09-15"},"accession":"2467472","cross_references":{"Australian New Zealand Clinical Trials Registry":["ACTRN12618001075279"]}}