[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651290":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":38,"responsibleParty":53,"collaborators":26,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":57,"sex":63,"minAge":64,"maxAge":26,"enrollmentInfo":65,"targetDuration":26,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":74,"overallStatus":41,"whyStopped":26,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"Mackay Memorial Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Slow Jogging Exercise Group","EXPERIMENTAL","Participants assigned to this arm will receive a standardized 12-week slow jogging exercise program in addition to usual care. The intervention includes slow jogging at least three times per week, standardized exercise instruction, an educational manual, an exercise demonstration video, exercise logs, and regular follow-up through the official LINE account to promote adherence. Outcome assessments will be conducted at baseline and at weeks 4, 8, and 12.",[13],"Behavioral: Slow Jogging Exercise",{"label":15,"type":16,"description":17,"interventionNames":18},"Usual Care Group","ACTIVE_COMPARATOR","Participants assigned to this arm will receive usual care, including routine health education and sleep education provided by the hospital. Educational materials and follow-up will be delivered according to standard clinical practice. After completion of the study, participants will receive the slow jogging educational materials.",[19],"Behavioral: General Health and Sleep Education",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Slow Jogging Exercise","Participants assigned to the intervention group will receive a standardized 12-week slow jogging exercise program in addition to usual care. Participants will perform slow jogging at least three times per week, with each session lasting approximately 36 minutes and allowing accumulation in bouts of at least 15 minutes. Before starting the intervention, participants will receive standardized face-to-face instruction, an educational manual, and an exercise demonstration video. The principal investigator will provide practical training, verify participants' exercise technique and safety, and confirm competency before home-based exercise begins. Participants will record each exercise session in an exercise diary and receive regular reminders and follow-up through the official LINE account to promote adherence. Outcome assessments will be conducted at baseline and at weeks 4, 8, and 12.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"General Health and Sleep Education","Participants assigned to the control group will receive routine health education and sleep education provided by the hospital. Educational messages will be delivered through the official LINE account during the study period. After completion of the study, participants will receive the slow jogging educational materials.",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":36,"email":37},"Hsin-Yi Ku, RN, MSN","CONTACT","+886-2-2543-3535","3991","shinyi.6178@mmh.org.tw",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":26},"Taipei Mackay Memorial Hospital","RECRUITING","Taipei","Taipei City","10449","Taiwan","TW",{"type":48,"coordinates":49},"Point",[50,51],121.52639,25.05306,{"lat":51,"lon":50},{"type":54,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100651290","slow-jogging-for-breast-cancer-survivors-100651290",false,"NCT07757763","Slow Jogging for Breast Cancer Survivors","The Effectiveness of Slow Jogging on Sleep, Fatigue, and Quality of Life in Breast Cancer Survivors","SJBC","Inclusion Criteria\n\n1. Female breast cancer survivors aged 20 years or older.\n2. Histologically confirmed hormone receptor-positive breast cancer (Stage I-IV) and considered suitable for exercise intervention by the treating physician.\n3. Completed primary cancer treatment (surgery, chemotherapy, or radiotherapy) within the previous 12 months; participants receiving ongoing anti-HER2 targeted therapy and\u002For endocrine therapy are eligible.\n4. Able to independently operate a smartphone and willing to install and use the study application.\n5. Self-reported sleep disturbance within the previous two weeks, defined as a Single-item Sleep Quality Scale (SQS) score ≥ 6.\n6. Willing to participate and provide written informed consent.\n\nExclusion Criteria\n\n1. History of cancer treatment-related cardiovascular complications or judged by the treating physician to be unsuitable for exercise.\n2. Musculoskeletal disorders affecting lower-extremity function (e.g., plantar fasciitis, knee osteoarthritis, ankle degenerative disease) that limit exercise participation.\n3. Currently participating in another structured moderate- or vigorous-intensity aerobic exercise program (≥3 sessions\u002Fweek, ≥30 minutes\u002Fsession for ≥3 consecutive weeks).\n4. Any other medical or psychological condition judged by the investigator to interfere with safe participation or completion of the study.","FEMALE","20 Years",{"count":66,"type":67},104,"ESTIMATED","INTERVENTIONAL",[70],"NA","Breast cancer survivors frequently experience persistent sleep disturbance, cancer-related fatigue, and reduced health-related quality of life after completion of primary treatment. Although exercise is recommended as an important component of survivorship care, evidence regarding the effectiveness of slow jogging remains limited. This investigator-initiated, single-center, parallel-group randomized controlled trial aims to evaluate the effectiveness of a standardized 12-week slow jogging exercise program in women aged 20 years or older with hormone receptor-positive Stage I-IV breast cancer who have completed primary cancer treatment within the previous 12 months. Participants will be randomized using permuted block randomization (block size = 6) to receive either a slow jogging intervention plus usual care or usual care alone. The primary outcome is sleep quality measured by the Chinese Pittsburgh Sleep Quality Index (CPSQI). Secondary outcomes include cancer-related fatigue measured by the Taiwanese Brief Fatigue Inventory (BFI-T) and health-related quality of life measured by the Functional Assessment of Cancer Therapy-Breast (FACT-B). Outcomes will be assessed at baseline and at Weeks 4, 8, and 12.",[73],"Breast Neoplasms",[75,76,77,78,79,80,81],"Breast Cancer Survivors","Slow Jogging","Exercise Therapy","Sleep Quality","Cancer-Related Fatigue","Quality of Life","Randomized Controlled Trial","2026-08-06",{"date":84,"type":85},"2026-08-11","ACTUAL",{"date":87,"type":85},"2026-04-14",{"date":89,"type":67},"2027-01-31",{"name":5,"class":6},1]