[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Dalarna University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":129},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,71,107],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":5},"100481519","structured-contraceptive-counseling-during-pregnancy-100481519",false,"NCT05550064","Structured Contraceptive Counseling During Pregnancy","Evaluating Effects of Prepartum Structured Contraceptive Counseling to Increase Postpartum Use of Long-acting Reversible Contraception","Inclusion Criteria:\n\n* 18 years or older, gestational week 30 or more, need for contraception 6 months or more after delivery\n\nExclusion Criteria:\n\n\\- Language barrier that affects participation when an interpreter is not available, assisted fertilization, planned sterilization of partner, use of contraception for other purposes than pregnancy prevention.",true,"FEMALE","18 Years",{"count":20,"type":21},160,"ESTIMATED","INTERVENTIONAL",[24],"NA","Unintended pregnancy is common among women of fertile age, and also among those who have recently given birth. A Swedish study has shown that about 7.7% experience a new pregnancy, and that 2.5% will have an abortion between 12-24 months from childbirth.\n\nThis is a prospective observational intervention study, aiming to evaluate the effects of structured contraceptive counseling during pregnancy on uptake of contraception postpartum and more specifically on long-acting reversible contraceptive methods, and to identify and explore the provider's and patient's experiences of structured contraceptive counseling during pregnancy.",[27,28,29,30,31],"Contraception","Intrauterine Device","Contraceptive Implant","Long-acting Reversible Contraception","Counseling","RECRUITING","2025-09-03",{"date":35,"type":36},"2025-09-10","ACTUAL",{"date":38,"type":36},"2022-11-19",{"date":40,"type":21},"2026-12",{"name":42,"class":43},"Dalarna University","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":70},"100439989","evisualisation-of-physical-activity-and-pain-evis-for-patients-with-chronic-pain-100439989","NCT05009459","eVISualisation of Physical Activity and Pain (eVIS) for Patients With Chronic Pain","eVISualisation of Physical Activity and Pain (eVIS) for Patients With Chronic Pain Participating in Swedish Interdisciplinary Pain Rehabilitation Programs: a Registry-based Randomized Controlled Clinical Trial","eVIS","Inclusion Criteria:\n\nSwedish IPRP treatment criterias will be applied as patients entering the trial must be accepted for IPRP: Principal IPRP inclusion criteria are:\n\n* persistent or intermittent pain lasting ≥3 months\n* pain affecting daily activities to a large extent,\n* completed systematic assessment and non-pharmacological optimization is completed,\n* screening for psychosocial risk factors and differential diagnosis completed\n\nIn addition the following criterias will be appled:\n\n* Patients aged 18-67 years.\n* Patients must be able to hear, see, and comprehend spoken and written Swedish\n* Daily access to a computer, smartphone, or tablet.\n\nExclusion Criteria:\n\n* Patients who need to use a walking aid indoors.\n* Patients living with pain caused by systemic disease or malignancies.","ALL","67 Years",{"count":55,"type":21},280,[24],"Introduction: Living with chronic pain often involves negative consequences. Interdisciplinary Pain Rehabilitation Programs (IPRPs), a subset of Interdisciplinary Treatment (IDT) includes physical activity and exercise and is considered superior to single-treatment measures in patients with chronic pain. However, effects emerge sub-optimal and as many as 30% of patients deteriorate in some outcomes. A novel intervention, eVISualisation (eVIS) of physical activity and pain, has been systematically developed to facilitate patients in reaching and maintaining recommended individualized physical activity levels. The aim is to transparently report on methodology, outcome assessments, and processes for a registry-based randomized controlled trial (R-RCT) initiated as an internal pilot study.\n\nMethods and analysis: The R-RCT will recruit approximately 400 patients with chronic pain who are registered at primary and specialized IPRP units (n=15) in Sweden. Participants will be randomly allocated to either an IPRP + eVIS or the control group that will receive only IPRP treatment. eVIS entails objectively measured physical activity (steps) and patient-reported outcomes (pain intensity, affect on daily activities, pharmaceutical consumption) collected and visualized in the web application PATRON. Data from an initial 30 participants completing the study period (6 months) will be included in a pilot study designed to evaluate recruitment- and randomization processes, standardized effect size, sample size, characteristics of outcomes, follow-up rates of the R-RCT. Outcome variables will be extracted from PATRON and from six national registries. Multivariate statistics and repeated measures analyses will be performed. Quality Adjusted Life Years (QALYs) and Incremental Cost Effectiveness Ratio (ICER) will be calculated for cost effectiveness evaluation.\n\nEthics\u002Fdissemination: The Swedish Ethics Review Board granted approval (Dnr 2021\u002F02109). Results will be disseminated through peer-review journals.",[59],"Chronic Pain",[61],"Chronic pain Registry-based randomized clinical trial","2025-08-22",{"date":64,"type":36},"2025-08-28",{"date":66,"type":36},"2021-10-28",{"date":68,"type":21},"2026-12-31",{"name":42,"class":43},1,{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":16,"sex":52,"minAge":78,"maxAge":79,"enrollmentInfo":80,"targetDuration":4,"studyType":82,"phases":4,"briefSummary":83,"conditions":84,"keywords":91,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},"100507909","uppsala-dalarna-dementia-and-gait-project-100507909","NCT05893524","Uppsala-Dalarna Dementia and Gait Project","UDDGait™","Inclusion Criteria:\n\n* Patients undergoing memory assessment at at Uppsala University Hospital, Sweden\n* Patients undergoing memory assessment at at Falu Hospital, Sweden\n* Cognitively unimpaired individuals with a Mini Mental State Examination (MMSE) score of \\> 26\n\nExclusion Criteria:\n\n* Inability to walk three meters back and forth\n* Inability to rise from a sitting position\n* Indoor use of a walking aid\n* Current or recent hospitalization (within the last 2 weeks)\n* Need of an interpreter to communicate in Swedish","37 Years","94 Years",{"count":81,"type":21},550,"OBSERVATIONAL","UDDGait™ is a multidisciplinary research project with the overreaching goal of providing an aid for early identification of cognitive impairment and risk of dementia development, thereby providing a basis for adequate symptom relieving and health promoting interventions.\n\nA new concept is investigated for this purpose: a \"dual-task-test\", which implies the combination of a well-established mobility test (Timed Up-and-Go, TUG) with a simultaneous verbal task (i.e. TUG dual-task, TUGdt). This type of test has been judged as a potential aid for early identification of dementia disease. More research is needed to further examine the test's validity, reliability and predictive capacity.\n\nThe overall aim is to investigate if TUGdt is useful as an aid for prediction of dementia disease. To ensure the results, the aim is also to evaluate the test's measurement properties and to generate normative reference values of healthy control persons.",[85,86,87,88,89,90],"Dementia","Dementia, Mixed","Dementia Senile","Dementia of Alzheimer Type","Mild Cognitive Impairment","Subjective Cognitive Impairment",[92,93,94,85,89,90,95,96,97],"Timed Up-and-Go, TUG","TUG dual-task","Cognitive tests","Alzheimer's disease","Step parameters","Video recorded tests","2025-02-11",{"date":100,"type":36},"2025-02-12",{"date":102,"type":36},"2015-04-09",{"date":104,"type":21},"2026-12-24",{"name":42,"class":43},2,{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":114,"targetDuration":4,"studyType":22,"phases":116,"briefSummary":117,"conditions":118,"keywords":4,"overallStatus":120,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":4},"100522697","nynnamm---effects-of-infant-directed-singing-on-breastfeeding-difficulties-100522697","NCT06085989","Nynnamm - Effects of Infant Directed Singing on Breastfeeding Difficulties","Nynnamm","Inclusion Criteria:\n\n* Mothers who seek support for breastfeeding difficulties.\n* Mothers who seek support for experiencing a low milk supply.\n* Mothers who seek support for sore nipples.\n* Mothers who seek support for breast pain.\n* Mothers who seek support for feeling stressed.\n* Mothers who seek support for feeling unwell while breastfeeding.\n* Mothers who seek support for having an infant who has problems with latching the breast.\n* Must understand Swedish or English.\n* Must be over 18 years old.\n\nExclusion Criteria:\n\n* Living outside Region Dalarna, Sweden\n* Living outside Region Uppsala, Sweden\n* Living outside Region Värmland, Sweden",{"count":115,"type":21},260,[24],"Breastfeeding is one of the most effective, health economical interventions to promote health and reduce illness in both mothers and children. However, breastfeeding in Sweden is under threat. An increasing number of newborns will miss out on its benefits because lack of lactation support for mothers with breastfeeding difficulties, which is the main reasons for breastfeeding cessation. About 110,000 mothers breastfeed every year but the prevalence is decreasing. Many mothers are dissatisfied with the support they receive from health care. Maternal infant-directed singing could be an effective, person- and family-centered, cost-effective, self-care intervention to reduce stress and breastfeeding difficulties in new mothers as well as increasing oxytocin, which is an important hormone for lactation and well-being.\n\nThis project evaluates the effect of a self-care intervention involving maternal infant-directed singing during breastfeeding on maternal stress, experiences, and breastfeeding rates up to six months postpartum among mothers with breastfeeding difficulties. The mothers are randomized to standard care and infant-directed singing or control with standard care. The primary outcome is the proportion of breastfeeding four weeks after the intervention. 260 mothers will be included in the project, which will be conducted during 2024-2025, and data will be analyzed and presented in 2026. A data management plan will ensure that all research activities are well organized.",[119],"Breastfeeding","NOT_YET_RECRUITING","2023-10-10",{"date":123,"type":36},"2023-10-17",{"date":125,"type":21},"2024-01-01",{"date":127,"type":21},"2028-12-31",{"name":42,"class":43},""]