[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universidad Pedagógica y Tecnológica de Colombia\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":51},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100612541","three-brief-psychological-interventions-for-acute-pain-in-inpatients-in-boyac-100612541",false,"NCT07254923","Three Brief Psychological Interventions for Acute Pain in Inpatients in Boyacá","Three Brief Psychological Interventions for Acute Pain in Inpatients in Boyacá: Randomized Three-Arm Clinical Trial","Inclusion Criteria:\n\n* Age ≥18 years.\n* Admitted to short-stay inpatient or emergency observation units at participating hospitals (same index admission).\n* Acute pain ≤7 days with baseline pain ≥4\u002F10 on a 0-10 numeric\u002Fvisual scale.\n* Clinically stable and able to remain at bedside for \\~30-40 minutes (consent, baseline, single session, post-session assessment).\n* Analgesic regimen stable ≥1 hour before baseline pain rating (no planned change during the \\~20-minute study window unless clinically required).\n* Able to understand simple instructions and communicate pain ratings (verbal or pointing) and to provide written informed consent.\n\nExclusion Criteria:\n\n* Cancer-related pain or chronic pain \\>6 months (e.g., widespread musculoskeletal pain\u002Ffibromyalgia).\n* Active inflammatory\u002Fdegenerative rheumatic disease causing ongoing daily pain that would confound acute pain ratings (e.g., rheumatoid arthritis flare, advanced osteoarthritis, severe osteoporosis-related pain).\n* Cognitive impairment\u002Fdementia, delirium, or acute severe psychiatric disturbance that prevents consent or reliable self-report.\n* Respiratory conditions that contraindicate slow deep-breathing rescue (e.g., decompensated COPD, acute asthma, need for high-flow oxygen or ventilatory support).\n* Hemodynamic or clinical instability (e.g., need for urgent procedure; in resuscitation\u002Freanimation area; RASS ≤ -3; MAP \\\u003C65 mmHg or SBP \\\u003C90 mmHg; SpO₂ \\\u003C90% despite usual oxygen) at screening.\n* Participation in another interventional study targeting pain during the same admission.\n* Refusal to participate or withdrawal of consent.","ALL","18 Years","90 Years",{"count":20,"type":21},160,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study evaluates two brief, non-drug psychological techniques-body-scan mindfulness and guided imagery\u002Fdistraction-delivered as a single bedside session to reduce acute pain in adults admitted to short-stay inpatient wards or emergency observation units in Boyacá, Colombia. Participants are randomly assigned (1:1:1) to body-scan mindfulness, guided imagery\u002Fdistraction, or a brief cognitive-behavioral psychoeducation session (active comparator). Each session lasts under 20 minutes and usual medical care continues. Pain intensity (0-10) is recorded within 5 minutes before the session and within 2 minutes after completion on the same day. If pain remains very high (e.g., ≥8-9\u002F10) or the activity cannot be completed, up to 5 minutes of supervised slow deep-breathing may be offered as rescue, and the clinical team may adjust analgesics per routine care. Secondary measures (specified in Outcome Measures) include patient satisfaction, feasibility (session duration and completion), use of rescue measure, and adverse events; exploratory data may include short-term psychological scales collected by a blinded assessor and the association with length of stay during the current admission. Adults aged ≥18 years with acute pain ≤7 days and baseline pain ≥4\u002F10 may be eligible. The study takes place across four public hospitals in Boyacá, Colombia.",[27,28],"Pain Management","Pain Acute",[30,31,32,33,34,35,27,36,37],"body scanning","ABC","Guided Imagery","Breathing Exercises","Acute Pain","Pain Measurement","Inpatients","Randomized Controlled Trial","NOT_YET_RECRUITING","2025-11-19",{"date":41,"type":42},"2025-11-28","ACTUAL",{"date":44,"type":21},"2026-01",{"date":46,"type":21},"2026-12-16",{"name":48,"class":49},"Universidad Pedagógica y Tecnológica de Colombia","OTHER",4,""]