[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"return-to-work\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:return-to-work":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,62,99,125,157,192,226],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":41,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":50,"lastUpdatePostDateStruct":51,"startDateStruct":54,"completionDateStruct":56,"leadSponsor":58,"locationsCount":61},"100636162","develop-and-evaluate-an-artificial-intelligence-assisted-prehabilitation-program-for-returning-to-work-and-cost-effectiveness-analysis-in-patients-with-oral-cancer-100636162",false,"NCT07562100","Develop and Evaluate An Artificial Intelligence Assisted Prehabilitation Program for Returning to Work and Cost-effectiveness Analysis in Patients With Oral Cancer","Inclusion Criteria:\n\n* Adult (\\> 20 years old and younger than 70 years old)\n* Newly diagnosed as OC and scheduled to receive cancer-related treatment\n* Able to use Mobile phone\n* Willing to sign an informed consent form after receiving a detailed explanation of the study's aims and procedures\n* Healthcare professionals involved in patients' care, including doctors, nurses, case managers, dietitians, rehabilitation therapists, and psychologists\n* Family members who are primary caregivers of the participating patients, engaged in different stages of medical care\n\nExclusion Criteria:\n\n* Risk populations for walking or performing exercise\n* Patients with cognitive impairment or psychiatric diseases",true,"ALL","20 Years","70 Years",{"count":20,"type":21},650,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to develop and evaluate an Artificial Intelligence Assisted Prehabilitation Program (AI APP) for returning to work and cost-effectiveness analysis in patients with oral cancer (OC). The main questions it aims to answer are:\n\n* What kinds of needs are related to returning to work (RTW) in patients with OC from diagnosis to survival that we can incorporate into the development of AI APP to assist this population ?\n* How is the effect of the AI APP that based on findings from the first question for patients with OC on physical and psychological distress, fear of recurrence, self-efficacy in coping with cancer, communication, motor function, quality of life, and RTW?\n* How is the effect of the RTW AI prediction model to identify high-risk groups ? And how is the comprehensive cost effectiveness of benefits and quality of life of the AI APP for OC population?\n\nResearchers will compare patients without using AI APP to see if the AI APP works to assist with coping physical and psychological distress, communication, motor function, quality of life, and RTW issues for individuals with OC?\n\nParticipants will:\n\n* Be asked to fulfill a structural questionnaire, or engage in a semi-structured one-by-one interview or a focus group to assess their physical, psychological, and social support needs in the first stage.\n* Be invited to participant the pilot testing of AI APP in the second stage.\n* Be provided and trained by 3-month AI APP for 3 months or cared as usual in the third stage.\n* Complete a structural questionnaire and follow up one year, including the baseline (before using the AI app) and at 1-2 weeks, 3 months, 6 months, 9 months, and 12 months after the baseline.\n* Engage in one-by-one interview or a focus group to assess user experiences of the AI APP.",[27,28,29,30,31,32,33,34,35,36,37,38,39,40],"Oral Cancer","Psychological Distress","Communication Aids for Disabled","Physiotherapy","Return to Work","Prehabilitation","Physical Symptom Distress","Motor Function","Rehabilitation","Quality of Life","Cost Effectiveness","Artifical Intelligence","Prediction Model","Case Management, APP(Application)",[42,31,27,28,29,30,32,43,44,35,45,46,47,48],"Artificial Intelligence","Physical symptom distress","motor function","Quality of life","Cost effectiveness","prediction model","case management, APP(Application)","RECRUITING","2026-04-24",{"date":52,"type":53},"2026-05-01","ACTUAL",{"date":55,"type":53},"2024-09-27",{"date":57,"type":21},"2029-12-01",{"name":59,"class":60},"Taipei Veterans General Hospital, Taiwan","OTHER_GOV",5,{"id":63,"slug":64,"hasResults":11,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":68,"eligibilityCriteria":69,"healthyVolunteers":11,"sex":16,"minAge":70,"maxAge":18,"enrollmentInfo":71,"targetDuration":4,"studyType":22,"phases":73,"briefSummary":74,"conditions":75,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":98},"100632971","evaluation-of-the-addpro-vocational-reintegration-program-add-pro-eval-100632971","NCT07520617","Evaluation of the ADD'Pro Vocational Reintegration Program (ADD-PRO-EVAL)","Evaluation of the ADD'Pro Program: A Partnership-Based Approach to Support Vocational Reintegration of Patients Receiving Addiction Care (ADD-PRO-EVAL)","ADD-PRO-EVAL","Inclusion Criteria:\n\n* Adult of working age (18 years or older)\n* Diagnosed substance use disorder receiving medical care\n* Unemployed or on sick leave with a vocational reorientation project\n* Motivated to work in the competitive labour market\n* Living in or wishing to work in the Puy-de-Dôme department (63), France\n* Legally authorised to work\n* Capable of providing written informed consent\n* Affiliated with a French social security scheme\n\nExclusion Criteria:\n\n* Medical care provided under a court-ordered treatment obligation\n* Previously included in the ADD'Pro program\n* Residing outside the Puy-de-Dôme with no plan to work in the department\n* Under legal guardianship (tutelle, curatelle, or sauvegarde de justice)\n* Deprived of liberty","16 Years",{"count":72,"type":21},100,[24],"The goal of this clinical trial is to evaluate whether an integrated medico-psychosocial vocational support program (ADD'Pro) can improve employment outcomes in adults with substance use disorders receiving care at a specialized addiction day hospital.\n\nThe main question it aims to answer is:\n\n\\- Does participation in the ADD'Pro program increase the rate of competitive employment (at least one day worked in the open labour market) at 6 months compared to standard employment services?\n\nResearchers will compare participants enrolled in the ADD'Pro program to participants referred to conventional employment services (France Travail or Cap Emploi) to see if structured, dual medico-psychosocial support leads to higher rates of vocational reintegration, better employment preparation, improved quality of life, and reduced physiological stress reactivity.\n\nParticipants will:\n\n* Be randomly assigned to either the ADD'Pro program or standard employment services\n* If assigned to ADD'Pro: receive immediate individualised support from a vocational counsellor (CIP) at the CeCler Association, running in parallel with their hospital addiction care, with no fixed end date\n* If assigned to standard care: be referred to conventional employment services with monthly follow-up interviews at the hospital, and the option to join ADD'Pro after 6 months\n* Complete structured interviews and validated questionnaires at inclusion, 3, 6, and 12 months\n* A sub-sample of up to 50 participants will additionally take part in a simulated job interview stress test (adapted TSST) with salivary biomarker collection and heart rate monitoring at inclusion and 6 months",[76,77,78,31,79,80,81,82,83,84,85,86],"Addiction","Addiction Disorders","Substance Use Recovery","Recovery","Recovery Outcomes","Substance Use Disorder (SUD)","Employment, Supported","Employment","Substance Related Disorders","Vocational Rehabilitation","Substance Use (Drugs, Alcohol)","NOT_YET_RECRUITING","2026-04-02",{"date":90,"type":53},"2026-04-09",{"date":92,"type":21},"2026-04",{"date":94,"type":21},"2029-04",{"name":96,"class":97},"University Hospital, Clermont-Ferrand","OTHER",1,{"id":100,"slug":101,"hasResults":11,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":105,"eligibilityCriteria":106,"healthyVolunteers":11,"sex":16,"minAge":107,"maxAge":4,"enrollmentInfo":108,"targetDuration":4,"studyType":110,"phases":4,"briefSummary":111,"conditions":112,"keywords":4,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":98},"100625175","professional-impact-of-osteoarticular-trauma-100625175","NCT07419217","Professional Impact of Osteoarticular Trauma","Professional Impact of Osteoarticular Trauma: Retrospective Study on Return to Work, Accommodations, and Recognition in the Workplace","IPTO","Inclusion Criteria:\n\n* Adults who were treated for osteoarticular trauma at the hospital between June 2021 and June 2024\n* Patients who were employed prior to the injury\n\nExclusion Criteria:\n\n* Death or major disability preventing completion of the questionnaire\n* Protected persons\n* Refusal to participate or no contact after follow-up\n* Patients who were unemployed prior to the trauma","18 Years",{"count":109,"type":21},200,"OBSERVATIONAL","This study aims to describe the medical, social, and organizational determinants of returning to work after an osteoarticular injury, particularly limb fractures.\n\nUsing observational data, the study will evaluate the modalities of returning to work within 12 months of the injury and analyze the factors influencing professional reintegration, including the severity of the injury, functional recovery, pain, professional characteristics, workplace accommodations, and administrative support measures such as recognition of disabled worker status.\n\nThe study will also explore the point at which the issue of returning to work is first raised with the patient during hospitalization, a period during which professional reintegration is often insufficiently anticipated. By identifying current practices and breaking points, this study aims to improve understanding of the pathways to returning to work in the context of the healthcare system and the world of work in France.",[35,31,113,114,115,85],"Occupational Health\u002FMedicine","Work Capacity Evaluation","Disabled Persons","2026-02-20",{"date":118,"type":53},"2026-02-23",{"date":120,"type":21},"2026-02-18",{"date":122,"type":21},"2027-02-02",{"name":124,"class":97},"Hopitaux de Saint-Maurice",{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":15,"sex":16,"minAge":107,"maxAge":4,"enrollmentInfo":131,"targetDuration":4,"studyType":22,"phases":133,"briefSummary":134,"conditions":135,"keywords":138,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":98},"100584412","in-vitro-exposure-by-vr-to-enhance-return-to-work-after-sick-leave-due-to-mental-health-related-complaints-100584412","NCT06888999","In Vitro Exposure by VR to Enhance Return to Work After Sick Leave Due to Mental Health Related Complaints","Inclusion Criteria:\n\n\\- sick listed cabin crew with mental health related complaints that are referred by the occupational physician to a specific psychotherapist practice\n\nExclusion Criteria:\n\n* epilepsy\n* vestibular disorder\n* no signed informed consent",{"count":132,"type":21},118,[24],"The goal of this pilot randomised controlled trial is to investigate whether in vitro exposure by VR enhances return to work (RTW) in flight cabin crew on sick leave with mental health related complaints. The main research questions are: 1. Does VR enhances time to RTW? 2. Does VR increase self-efficacy and positive cognitions regarding RTW, and decrease job anxiety? Researchers will compare a control group receiving care as usual as provided by the occupational physician and a psychologist to an intervention group receiving care as usual plus (al least) one session with VR-glasses in which participants are virtually exposed to their workplace.",[31,136,137],"Occupational Stress","Self-Efficacy",[139,140,141,142,143,144,145,146,147],"virtual reality","return to work","pilot randomized controlled trial","cabin crew","stress","return to work self-efficacy","job anxiety","usability","return to work attitude","2026-01-08",{"date":150,"type":53},"2026-01-09",{"date":152,"type":53},"2025-11-17",{"date":154,"type":21},"2027-03",{"name":156,"class":97},"Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)",{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":163,"eligibilityCriteria":164,"healthyVolunteers":11,"sex":16,"minAge":70,"maxAge":4,"enrollmentInfo":165,"targetDuration":4,"studyType":22,"phases":167,"briefSummary":168,"conditions":169,"keywords":177,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":183,"lastUpdatePostDateStruct":184,"startDateStruct":186,"completionDateStruct":188,"leadSponsor":190,"locationsCount":98},"100613601","assess-the-efficacy-of-tailored-patient-information-and-voluntary-patient-managed-outpatient-digital-follow-up-i-pod-as-an-adjunct-to-standard-treatment-according-to-national-guidelines-in-the-national-trauma-plan-among-adult-trauma-patients-in-norway-100613601","NCT07268716","Assess the Efficacy of Tailored Patient Information and Voluntary Patient-managed Outpatient Digital Follow-up (I-POD) as an Adjunct to Standard Treatment According to National Guidelines in the National Trauma Plan Among Adult Trauma Patients in Norway.","A Randomized Controlled Clinical Trial to Assess the Efficacy of Tailored Patient Information and Voluntary Patient-Managed Outpatient Digital Follow-Up as an Adjunct to Standard Treatment According to National Guidelines in Adult Trauma Patients in Norway (The POSTRAUMA Trial).","POSTRAUMA","Inclusion Criteria:\n\n* 16 years or older\n* Fulfils the national criteria for TTA and admitted to HUS following trauma\n* Included in NTR database\n* Able to give informed consent\n\nExclusion Criteria:\n\n* 15 years or younger\n* Not included in NTR database\n* Deceased before discharge from the hospital.\n* Not able to give informed consent\n* Insufficient command of the Norwegian language\n* Foreign tourists or nationals\n* Suicide attempt or serious self-inflicted trauma\n* Serious psychiatric disorders or serious ongoing substance abuse",{"count":166,"type":21},256,[24],"The POSTRAUMA trial is a clinical trial at The Regional trauma centre of Western Norway, Haukeland University Hospital.\n\nTrauma is the leading cause of death worldwide in patients aged 1-45 years. In Norway, approximately 10,000 patients are admitted to hospital annually due to trauma, with 66% being male. The mean age is 43 years for male and 48 years for female, indicating a relatively young patient population.\n\nWhile mortality rates are decreasing, a significant proportion of trauma survivors experience long-term disabilities, reduced quality of life, and difficulties in returning to work. These consequences impose substantial burdens on individuals, families, and society. Considering these issues, a shift in focus is needed-from survival alone to long-term functional recovery and quality of life after trauma.\n\nSevere trauma often requires long-term follow-up, both physically and psychosocially. Traditional follow-up can be fragmented and not tailored to individual needs. Digital patient monitoring and tailored information have the potential to improve patient pathways, but knowledge about how these are experienced by patients is limited.\n\nThe goal is to find out if Norwegian trauma patients who receive tailored patient information and patient-managed outpatient digital follow-up, in addition to standard treatment have:\n\n* Less disability\n* Return more often to work\n* Improved quality of life\n\nThe study population are Norwegian trauma patients, 16 years or older at date of inclusion, who are admitted to Haukeland University hospital (HUS) following trauma with trauma team activation. 256 patients will be included in this trial.\n\nParticipants will:\n\n* Answer a questionnaire at inclusion, one month, 6 months and 12 months.\n* Participants in the intervention group will be invited to digital outpatient follow up one month after the accident.\n* Some participants will be interviewed about how they experienced their trauma follow up.",[170,171,172,173,174,35,31,175,176],"Trauma Centers","Trauma Patients","Trauma (Including Fractures)","Trauma Injury","Rehabilitation After Neurological or Orthopaedic Injuries","HRQOL (Health Related Quality Of Life)","EQ5D5L-VAS",[178,179,180,140,181,182],"multitrauma","trauma","rehabilitation","HRQOL","EQ5D","2025-12-16",{"date":185,"type":53},"2025-12-22",{"date":187,"type":21},"2026-03-02",{"date":189,"type":21},"2029-12-31",{"name":191,"class":97},"Haukeland University Hospital",{"id":193,"slug":194,"hasResults":11,"nctId":195,"briefTitle":196,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":11,"sex":16,"minAge":107,"maxAge":199,"enrollmentInfo":200,"targetDuration":4,"studyType":22,"phases":202,"briefSummary":204,"conditions":205,"keywords":212,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":98},"100452609","phase-4-rehabilitation-for-survivors-of-out-of-hospital-cardiac-arrest-100452609","NCT05173740","Rehabilitation for Survivors of Out-of-hospital Cardiac Arrest","The ROCK Trial. A Multidisciplinary Rehabilitation Intervention Targeted Return-to-work in Sudden Out-of-hospital Cardiac Arrest Survivors A Pragmatic Randomised Controlled Trial","Inclusion criteria:\n\n* All adult survivors with first time out-of-hospital cardiac arrest\n* Discharged from the Hospitals will be assessed eligible for inclusion\n\nExclusion criteria:\n\n* Survivors who prior to the cardiac arrest were not part of the labour force with at least two years until they are qualified to receive retirement state pensions\n* Patients that cannot understand and fulfil the study surveys (in Danish)\n* Patients with short witnessed cardiac arrests with return of spontaneous circulation estimated less than 4 minutes and immediate awakening without ICU treatment","65 Years",{"count":201,"type":21},214,[203],"PHASE4","This study is a parallel group multicentre investigator-initiated clinical randomised controlled superiority trial that will include a total of 214 survivors of OHCA.\n\nParticipants will to be randomized with a 1:1 allocation ratio to either a intervention consisting of a comprehensive initiated tailored rehabilitation intervention focusing on supporting RTW plus usual care compared to usual care alone.",[206,207,208,31,209,35,210,211],"Cardiac Arrest","Heart Arrest","Cardiopulmonary Resuscitation","Return-to-work","Recovery of Function","Cardiac Rehabilitation",[213,214,207,208,215,209,216,35,210,211],"Labour marked","Cardiac arrest","Return to work","Back to Work","2025-12-01",{"date":219,"type":53},"2025-12-08",{"date":221,"type":53},"2022-02-01",{"date":223,"type":21},"2028-07-31",{"name":225,"class":97},"Rigshospitalet, Denmark",{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":232,"eligibilityCriteria":233,"healthyVolunteers":15,"sex":16,"minAge":107,"maxAge":234,"enrollmentInfo":235,"targetDuration":4,"studyType":22,"phases":237,"briefSummary":238,"conditions":239,"keywords":241,"overallStatus":49,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":252},"100557870","vitalwork-reintegration-program-for-employees-with-stress-related-complaints-100557870","NCT06543732","Vital@Work: Reintegration Program for Employees with Stress-related Complaints","Vital@Work: a Personalized Reintegration Program for Employees with Stress-related Complaints","Vital@Work","Inclusion Criteria:\n\n* Sick-listed employees from participating organisations (Amsterdam UMC, GGZ inGeest, Rijksschoonmaakorganisatie \\[RSO\\], and Transavia)\n* Aged 18-68\n* Between 2 and 12 weeks on sick leave\n* Suffering from stress-related complaints\n\nExclusion Criteria:\n\n* Non-sick-listed employees\n* Suffering from severe psychiatric disorders (e.g., suicidality, mania, psychosis, schizophrenia) or other chronic conditions (e.g., terminal illness) that could significantly affect the employee's mental health and, hence, prevent the return-to work process\n* Being pregnant or less than three months after delivery\n* Sick-listed for more than 12 weeks\n* Inability to complete either the eHealth modules or questionnaires\n* Presence of a legal conflict with the employer\n* Not signing informed consent","68 Years",{"count":236,"type":21},208,[24],"The objective of this study, Vital@Work reintegration program, is to support sick-listed workers with stress-related complaints in their return to work based on a personalized program. Therefore, the aim of this study is test whether participants supported by a tailored eHealth program, and if needed, additionally supported by a structured and stepwise Participatory Approach (PA) involving the sick-listed worker, their direct supervisor and a neutral party, show a faster and sustainable return to work as compared to participants in the control condition. This program is investigated in four different organizations, which differ in sector, size (small and large organizations), type of organization (private or public) and type of work.",[31,240],"Mental Health",[215,242,243],"Stress","Absenteeism","2025-01-28",{"date":246,"type":53},"2025-01-30",{"date":248,"type":53},"2025-01-08",{"date":250,"type":21},"2026-12-01",{"name":156,"class":97},4]