[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100602785":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":18,"locations":24,"responsibleParty":42,"collaborators":46,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":18,"eligibilityCriteria":54,"healthyVolunteers":51,"sex":55,"minAge":18,"maxAge":18,"enrollmentInfo":56,"targetDuration":18,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":26,"whyStopped":18,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"Universidad Rey Juan Carlos","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Moderate-Intensity Exercise","EXPERIMENTAL","The experimental group followed a structured five-week program combining moderate-intensity aerobic and resistance training, totaling 150 minutes per week, and supervised by physiotherapists. Exercise intensity was monitored using the Borg and OMNI-Res perceived exertion scales, with prior familiarization sessions provided. Adherence was supported through attendance tracking, reminder messages, and motivational feedback. Unlike previous studies focused on fatigue or quality of life, this protocol targeted pain modulation based on neurophysiological mechanisms. Sessions included step-based aerobic routines and resistance exercises with bands, with clear safety and effort guidelines in place. No drugs or devices were used during the intervention.",[13],"Other: Exercise",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group","NO_INTERVENTION","Participants maintained usual activities for five weeks without changing exercise habits. No additional interventions (drugs, devices, or procedures) were applied.",null,[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":18},"Exercise","The experimental group completed a five-week supervised program combining moderate-intensity aerobic and resistance training (150 min\u002Fweek). Intensity was monitored using the Borg and OMNI-Res scales after familiarization sessions. Adherence was encouraged through reminders, motivational messages, and follow-ups. Unlike prior studies, this intervention focused specifically on neurophysiological pain modulation. Sessions included step-based aerobic exercises and resistance training with elastic bands under safety protocols.",[9],[25],{"facility":5,"status":26,"city":27,"state":18,"zip":18,"country":28,"countryCode":29,"cosmosGeoPoint":30,"geoPoint":35,"contacts":36},"RECRUITING","Madrid","Spain","ES",{"type":31,"coordinates":32},"Point",[33,34],-3.70256,40.4165,{"lat":34,"lon":33},[37],{"name":38,"role":39,"phone":40,"phoneExt":18,"email":41},"Francisco Fernández, PhD","CONTACT","916 65 50 60","fasis.fernandez@urjc.es",{"type":43,"investigatorFullName":44,"investigatorTitle":45,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","DeAsís-Fernández, Francisco","Director",[47],{"name":48,"class":6},"Hospital General Universitario Gregorio Marañon","100602785","moderate-intensity-exercise-and-pain-sensitization-in-breast-cancer-survivors-a-case-based-study-100602785",false,"NCT07128030","Moderate-Intensity Exercise and Pain Sensitization in Breast Cancer Survivors: A Case-Based Study","Inclusion Criteria:\n\n* Adult women diagnosed with stage I-III breast cancer\n* Completion of active treatment (surgery, chemotherapy, and\u002For radiotherapy) at least 6 months prior to enrollment\n* Presence of persistent pain or altered sensation in the upper quadrant of the affected limb related to oncologic treatment\n\nExclusion Criteria:\n\n* Bilateral breast cancer\n* Locoregional recurrence\n* Other malignancies\n* Pre-existing pain not related to cancer treatment\n* Neurological or cognitive disorders\n* Non-Spanish speakers\n* Contraindications to moderate-intensity physical activity","FEMALE",{"count":57,"type":58},10,"ESTIMATED","INTERVENTIONAL",[61],"NA","The aim of this study was to evaluate the feasibility, safety, and acceptability of a supervised, combined moderate-intensity aerobic and resistance training program designed to reduce pain sensitization in BCS with persistent pain. Secondary objectives included assessing changes in pain intensity, somatosensory sensitivity, and temporal summation, while tertiary objectives focused on improvements in quality of life and functional capacity.",[64,65,66],"Exercise Training","Breast Cancer","Pain Management",[68,69,70,71],"pain severity","pain sensibilization","quantitative sensory testing","physical activity","2025-11-19",{"date":74,"type":75},"2025-11-24","ACTUAL",{"date":77,"type":75},"2025-08-23",{"date":79,"type":58},"2026-02-23",{"name":5,"class":6},1]