[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100522935":3},{"organization":4,"armGroups":7,"interventions":16,"overallOfficials":34,"centralContacts":38,"locations":44,"responsibleParty":81,"collaborators":83,"id":93,"slug":10,"hasResults":94,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":98,"eligibilityCriteria":99,"healthyVolunteers":94,"sex":100,"minAge":101,"maxAge":10,"enrollmentInfo":102,"targetDuration":10,"studyType":105,"phases":10,"briefSummary":106,"conditions":107,"keywords":111,"overallStatus":46,"whyStopped":10,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":123},{"fullName":5,"class":6},"University of California, San Francisco","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Newly diagnosed gynecologic cancer",null,"Participants will undergo physical function assessments, complete surveys, and medical records every 3 months +\u002F- 4 weeks prior to standard of care surgery (outside of this protocol). After surgery subjects will be followed for at least 3 months +\u002F- 4 weeks for up to one year after diagnosis. Medical record reviews will occur periodically to examine for long-term follow up oncologic outcomes of progression free survival, overall survival, and chemotherapy delays for up to 10 years after enrollment.",[13,14,15],"Other: Physical function assessment","Other: Self-reported Assessments and Questionnaires","Procedure: Surgery (Standard of Care, Non-Interventional)",[17,21,27],{"type":6,"name":18,"description":19,"armGroupLabels":20,"otherNames":10},"Physical function assessment","Physical assessments of frailty will be conducted in person.",[9],{"type":6,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"Self-reported Assessments and Questionnaires","Quality of life questionnaires and self-reported measures will be provided to complete during the course of the study",[9],[26],"Questionnaires",{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"PROCEDURE","Surgery (Standard of Care, Non-Interventional)","Surgical data will be reviewed via medical record",[9],[33],"Surgical Procedure",[35],{"name":36,"affiliation":5,"role":37},"Stephanie Cham, MD","PRINCIPAL_INVESTIGATOR",[39],{"name":40,"role":41,"phone":42,"phoneExt":10,"email":43},"Janet Titzler","CONTACT","415-353-9600","janet.titzler@ucsf.edu",[45,64],{"facility":5,"status":46,"city":47,"state":48,"zip":49,"country":50,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"RECRUITING","San Francisco","California","94143","United States",{"type":52,"coordinates":53},"Point",[54,55],-122.41942,37.77493,{"lat":55,"lon":54},[58,60,63],{"name":40,"role":41,"phone":42,"phoneExt":10,"email":59},"Janet.Titzler@ucsf.edu",{"name":10,"role":41,"phone":61,"phoneExt":10,"email":62},"877-827-3222","cancertrials@ucsf.edu",{"name":36,"role":37,"phone":10,"phoneExt":10,"email":10},{"facility":65,"status":46,"city":66,"state":67,"zip":68,"country":50,"cosmosGeoPoint":69,"geoPoint":73,"contacts":74},"Dana Farber Cancer Institute","Boston","Massachusetts","02215",{"type":52,"coordinates":70},[71,72],-71.05977,42.35843,{"lat":72,"lon":71},[75,79],{"name":76,"role":41,"phone":77,"phoneExt":10,"email":78},"Alexi Wright, MD, MPH","617-632-2334","Alexi_Wright@dfci.harvard.edu",{"name":80,"role":37,"phone":10,"phoneExt":10,"email":10},"Alexi Wright, MD MPH",{"type":82,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[84,86,88,91],{"name":85,"class":6},"Conquer Cancer Foundation",{"name":87,"class":6},"American Society of Clinical Oncology",{"name":89,"class":90},"National Institute on Aging (NIA)","NIH",{"name":92,"class":90},"Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)","100522935",false,"NCT06089083","PROmOting Gynecologic Cancer Patients With Frailty to Achieve Functional Recovery","PROmOting Gynecologic Cancer Patients With Frailty to Achieve Functional Recovery - PROOF Prospective Cohort Study","PROOF","Inclusion Criteria:\n\n* Age 18 years or greater\n* Undergoing evaluation for a newly diagnosed gynecologic malignancy\n* Ability of individual or legal guardian\u002Frepresentative to understand a written informed consent document, and the willingness to sign it\n\nExclusion Criteria:\n\n* Contraindication to any study-related procedure or assessment\n* Does not speak a language for which the consent form and study materials are available","FEMALE","18 Years",{"count":103,"type":104},500,"ESTIMATED","OBSERVATIONAL","This study seeks to understand how frailty, a term that describes people who are more vulnerable stressors such as a new medical problem, affects the outcomes and quality of life in adult patients with gynecologic cancer.",[108,109,110],"Malignant Female Reproductive System Neoplasm","Gynecologic Cancer","Gynecologic Neoplasm",[112,113],"Frailty","Risk Factors","2026-01-22",{"date":116,"type":117},"2026-01-26","ACTUAL",{"date":119,"type":117},"2023-10-18",{"date":121,"type":104},"2033-11-30",{"name":5,"class":6},2]