[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mobile-phone-use\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mobile-phone-use":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,48,78,105,131,159,182],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100636097","exploratory-investigation-of-the-acceptance-and-utility-of-14-day-trial-periods-and-application-related-outcome-measurement-abem-within-the-routine-prescription-of-the-diga-axia-100636097",false,"NCT07561255","Exploratory Investigation of the Acceptance and Utility of 14-day Trial Periods and Application-related Outcome Measurement (AbEM) Within the Routine Prescription of the DiGA Axia.","Real-world Quality Management Study With Axia to Evaluate the Measures of the DigiG (RAEMD Study)","RAEMD","Inclusion Criteria:\n\n* Willingness to use Axia.\n* Axia indication area.\n* Willingness to activate via onboarding brochure.\n\nExclusion Criteria:\n\n* Absence of the inclusion criteria","ALL","18 Years",{"count":20,"type":21},200,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective, multicenter, controlled real-world quality management study explores the acceptance and utility of two measures discussed in the context of the German Digital Act (DigiG) for the digital health application (DiGA) Axia: a 14-day trial period and an application-related outcome measurement (AbEM). Patients with axial spondyloarthritis in Axia's indication area who are eligible for prescription in routine care will receive one of two onboarding brochure versions in a 1:1 allocation: either the standard access procedure or immediate 14-day trial access until the health insurance activation code arrives. The manufacturer will analyze aggregated anonymized data to compare voucher redemption and app activation frequencies between groups and to assess acceptance and return rates of a voluntary five-item AbEM questionnaire at weeks 6 and 12. Secondary analyses will descriptively evaluate AbEM results and anonymized usage data.",[27,28],"Spondylitis, Ankylosing","Mobile Phone Use",[30,31,32,33,34,35],"axial spondyloarthritis","mobile health","digitalization","onboarding","real-world","therapeutic app","RECRUITING","2026-04-27",{"date":39,"type":40},"2026-05-01","ACTUAL",{"date":42,"type":40},"2026-04-10",{"date":44,"type":21},"2027-04-10",{"name":46,"class":47},"Wuerzburg University Hospital","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":62,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":77},"100537392","nutrition-care-in-patients-living-with-chronic-pain-100537392","NCT06277232","Nutrition Care in Patients Living With Chronic Pain","Developing Nutrition Care Integrated Into Pain Rehabilitation: a Feasibility and Non-Randomized, Controlled Quasi-Experimental Study","Inclusion Criteria:\n\n* Self reported Body Mass Index (BMI)\\>=25;\n* Written consent to participate and attend to the pain rehabilitation program due to disabling chronic pain (on sick leave or experiencing major interference in daily life due to chronic pain)\n* Agreement not to participate in other parallel treatments for weight reduction\n* Not currently using medications of weight reduction\n* Available to get access to internet via own mobile\u002Fcellphone.\n\nExclusion Criteria:\n\n* Health conditions such as pregnancy, active metabolic disease, rheumatoid arthritis, and serious psychiatric disease (investigator's judgement, eg, psychosis or suicidal ideation);\n* Coagulation disorders with predisposition to bleeding, medication with anticoagulants (low- dose aspirin is permitted);\n* hypersensitivity to anaesthetic\n* Difficulties in understanding the Swedish language.",{"count":20,"type":21},[24],"The investigators' purpose is to develop and test the feasibility, usability, and satisfaction of the Diet4painrelief app as a platform for implementing nutrition care in a specialist pain rehabilitation clinic. The Diet4painrelief will consist of two components: a) a screening tool for nutrition status b) an individually tailored behavior change program aiming to improve the dietary habits and behaviors of patients living with chronic pain.\n\nPart I: Included 20 patients with complex chronic pain to examine the feasibility and outcomes of evidence-based Interdisciplinary Pain Rehabilitation Program (IPRP) integrated with nutrition care. The Diet4painrelief includes a screening tool to assess basic nutritional status as well as their intake of key unhealthy and healthy foods and drinks (through three 24hour-dietary recordings or food diary). Thereafter, the patients receive a personalized behavior change program for dietary optimization. The investigators will design and adapt 6 modules in the digital platform (Diet4painrelief app) based on the International Association for the Study of Pain (IASP) recommendations (6 aspects about 'nutrition and pain') and Sweden's food culture. Clinical outcomes using patient-reported data on socio-demographics, pain aspects, psychometric data, physical disability, and quality of life will be measured at three occasions: first appointment (Pre-IPRP), immediately after completing the rehabilitation program (Post-IPRP), and at a 12-month follow-up (FU-IPRP). Blood samples will be taken to identify biomarkers at the same occasions that provide objective information on metabolic and nutritional abnormalities and further to evaluate the effect of the dietary intervention on changing of pain rehabilitation outcomes.\n\nPart II: Included 192 patients with complex chronic pain. Half of the participants receive IPRP and nutrition care (described above) and the other half receive standard IPRP.",[59,60,28,61],"Nutrition Poor","Overweight and Obesity","Pain, Chronic",[63,64,65,66],"Chronic pain","Nutrition care","Pain rehabilitation","eHealth","2026-02-13",{"date":69,"type":40},"2026-02-18",{"date":71,"type":40},"2024-08-01",{"date":73,"type":21},"2028-12-31",{"name":75,"class":76},"Linkoeping University","OTHER_GOV",1,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":84,"eligibilityCriteria":85,"healthyVolunteers":86,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":77},"100499272","investigating-baby-behavior-and-family-technology-use-study-100499272","NCT05781100","Investigating Baby Behavior and Family Technology Use Study","Maternal Technology Use During Feeding and Infant Self-Regulation and Growth","iBaby","Eligibility Criteria\n\nAt the time of recruitment, eligibility criteria for participants will include:\n\n* 18 years of age or older\n* In 3rd trimester of singleton pregnancy\n* History of healthy, low-risk pregnancy\n* Lives within 50 miles of the Cal Poly campus\n* Owns a mobile device\n\nAfter the child is born, eligibility criteria for participants will remain in the study will include:\n\n* Infant was born term (gestational age ≥37 weeks) Exclusion criteria include\n* Mother has an untreated medical or psychiatric condition (e.g. bipolar disorder) that could impede study participation or affect mother-infant interaction\n* Mother is participating in another interventional study that influences parenting, mother-infant interactions, feeding practices, or technology use\n* The mother is unwilling or unable to commit to longitudinal follow-ups of herself or her child\n* Infant was born preterm (gestational age \\\u003C37 weeks)\n* Infant diagnosed with fetal abnormality or medical condition that interferes with oral feeding (e.g., feeding disorder, milk protein allergy) or development\n* Infant diagnosed with developmental delay (e.g., Down's syndrome)",true,{"count":88,"type":21},345,[24],"Maternal sensitivity and contingent responsiveness to infant behavioral cues is an important contributor to infants' developing capacities to self-regulate. During early infancy, feeding interactions comprise a significant portion of mother-infant dyadic interactions and high-quality feeding interactions provide both nutritive and socioemotional benefits; recent data suggest that, for many dyads, mothers' sensitive responsiveness during feeding interactions is routinely impacted by the omnipresence of portable technology. The objective of the proposed research is to better understand the development and possible impacts of maternal technology use on infant feeding interactions, emotion and intake regulation, and sociobehavioral and growth outcomes.",[28,92,93,94,95],"Mother-Infant Interaction","Infant Development","Self-Regulation, Emotion","Self-Regulation","2025-02-21",{"date":98,"type":40},"2025-02-24",{"date":100,"type":40},"2023-01-16",{"date":102,"type":21},"2027-06-30",{"name":104,"class":47},"California Polytechnic State University-San Luis Obispo",{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":17,"minAge":112,"maxAge":18,"enrollmentInfo":113,"targetDuration":4,"studyType":22,"phases":115,"briefSummary":116,"conditions":117,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":77},"100523483","using-augmented-reality-to-promote-physical-activity-in-children-with-cerebral-palsy-100523483","NCT06096272","Using Augmented Reality to Promote Physical Activity in Children With Cerebral Palsy","A Pilot Study Using Exergaming With Augmented Reality to Promote Physical Activity in Children With Cerebral Palsy","Inclusion Criteria:\n\n* Diagnosis of cerebral palsy,\n* Ambulatory (GMFCS I and II)\n* English or Spanish speaking\n* No plans for lower extremity surgery in the next 4 months\n\nExclusion Criteria:\n\n* Moderate to severe developmental or cognitive delay\n* Significant hearing loss or visual impairment\n* Recent surgical procedure or fracture over the past 4 months that impacts physical activity","5 Years",{"count":114,"type":21},30,[24],"Children with cerebral palsy (CP), Gross Motor Functional Classification Scale (GMFCS) I-II will be recruited to participate in a home based physical activity intervention for 4 weeks. Demographic data will be collected, and validated surveys assessing baseline physical activity level and mobility will be completed. Participants will have an exercise program assigned and will be given a logbook to record their exercise adherence. They will be assigned to the Augment Reality (AR) app group. The AR app group will have exercises administered through the AR app. At the end of the program, participants will complete final surveys and an exit interview.",[118,28,119,120,121],"Cerebral Palsy","Pediatric ALL","Physical Disability","Physical Inactivity","2025-01-16",{"date":124,"type":40},"2025-01-20",{"date":126,"type":40},"2024-06-07",{"date":128,"type":21},"2025-09-01",{"name":130,"class":47},"Children's Hospital Los Angeles",{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":135,"acronym":4,"eligibilityCriteria":136,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":137,"enrollmentInfo":138,"targetDuration":4,"studyType":22,"phases":140,"briefSummary":141,"conditions":142,"keywords":145,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":77},"100572338","the-impact-of-using-mobile-games-on-rehabilitation-outcomes-in-thumb-rehabilitation-100572338","NCT06731972","The Impact of Using Mobile Games on Rehabilitation Outcomes in Thumb Rehabilitation","Inclusion Criteria:\n\n* Patients aged 18-65\n* With sufficient communication skills\n* Experiencing pain and functional impairment in the thumb (e.g., thumb fractures, tendon injuries, nerve injuries, osteoarthritis, trigger thumb, carpal tunnel syndrome, ligament injuries, soft tissue damage, etc.),\n* who are willing to volunteer.\n\nExclusion Criteria:\n\n\\- Illiteracy, lack of a smartphone, or the presence of neurological, orthopedic, or rheumatological chronic diseases in the affected limb.","65 Years",{"count":139,"type":21},38,[24],"Hand injuries and diseases are common reasons for hospital visits and lead to both functional and workforce losses, making them a persistent problem in treatment and rehabilitation approaches. Among the various functions of the hand, the thumb is of particular importance due to its large representation in the brain and its contribution to all gripping and holding functions. Loss of function in the thumb leads to a loss of at least 40% of hand skills. Therefore, restoring the thumb's original functionality is this study primary goal in rehabilitation. To achieve this goal, intensive rehabilitation is required, which cannot be fully accomplished through clinic sessions alone, as home exercises contribute significantly to this process. The low adherence of patients to home exercises has led researchers to explore various alternatives.\n\nThe aim of this study is to investigate the effect of mobile application games on rehabilitation outcomes in patients who have lost thumb function. For the pre- and post-treatment evaluations of the patients, the following assessment tools will be used: the Visual Analog Scale (VAS) for pain, the eight-shaped tape measure for edema, the Quick-DASH (Disabilities of the Arm, Shoulder, and Hand) scale for upper extremity functionality, a finger goniometer for joint range of motion, the DuruÖz Hand Index for measuring activities of daily living, and a home exercise adherence tracking form to evaluate adherence to home exercises.\n\nAs determined by this study power analysis, 38 patients with thumb injuries will be included in the study. These patients will be randomly assigned into two groups: the routine treatment group (19 patients) and the routine treatment plus mobile game group (19 patients). The routine treatment group will receive standard treatment at the Kırşehir Ahi Evran University Faculty of Physiotherapy and Rehabilitation Hand Clinic, including classical massage, stretching, functional exercises, electrical modalities, thermal agents, and home exercises. In the routine treatment plus mobile game group, in addition to the standard treatment, patients will engage in 20-30 minutes of mobile application games (e.g., Temple Run, Flappy Bird, Angry Birds) as part of their home exercise program.\n\nResearchers hypothesize that the group receiving mobile games in addition to the standard treatment will experience a better rehabilitation process in terms of thumb functionality, pain, and edema compared to the routine treatment group, and they will reach rehabilitation goals more quickly. Additionally, mobile games will increase motivation for home exercises and improve adherence. This study will be the first to examine the use of mobile games in thumb rehabilitation and their effect on adherence to home exercises. Researchers anticipate that the results of this study will inspire both clinicians and future research, reaching a wider audience through presentations and publications.",[143,144,28],"Thumb Injury","Rehabilitation Outcome",[146,147,148,149],"Thumb","Rehabilitation","Games","Technology","2024-12-09",{"date":152,"type":40},"2024-12-13",{"date":154,"type":40},"2024-05-15",{"date":156,"type":21},"2025-02-01",{"name":158,"class":47},"Kirsehir Ahi Evran Universitesi",{"id":160,"slug":161,"hasResults":11,"nctId":162,"briefTitle":163,"officialTitle":164,"acronym":4,"eligibilityCriteria":165,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":166,"targetDuration":4,"studyType":22,"phases":168,"briefSummary":169,"conditions":170,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":174,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":5},"100507867","instant-message-delivered-brief-internet-based-cognitive-behavioural-therapy-icbt-for-post-stroke-depression-100507867","NCT05892965","Instant Message-delivered Brief Internet-based Cognitive Behavioural Therapy (iCBT) for Post-stroke Depression","Instant Message-delivered Brief Internet-based Cognitive Behavioural Therapy (iCBT) for Post-stroke Depression: a Mixed Method Study","Inclusion Criteria:\n\n* Diagnosis of stroke (ICD-10 codes: I60-I69);\n* Aged ≥18;\n* Able to read and communicate in Chinese (Cantonese or Putonghua);\n* Able to use the text or voice messaging function on smartphone;\n* MoCA 5-minute Protocol (cognitive screen) ≥14;\n* Community-dwelling\n* Less than 1 year after stroke event;\n* PHQ-9 (depressive symptom) score ranging from 5 to 19 (note. mild: 5-9, moderate: 10-14, moderately severe: 15-19 and severe: 20-27)\n\nExclusion Criteria:\n\n* Diagnosis of psychiatric disease before stroke event or currently taking psychotropic drug including antidepressants\n* PHQ-9 ≥ 20 (i.e., severe depressive symptom)\n* Currently participating in any type of psychological intervention",{"count":167,"type":21},160,[24],"Around one third of stroke survivors develop depression at any point of time following the stroke event. Post-stroke depression (PSD) is associated with negative care outcomes including poorer function, longer hospital stays, increased outpatient and inpatient clinic use, and higher mortality rate. In Hong Kong (HK), the prevalence of PSD within the hospital setting was 36%, and up to 68% in the community setting. However, PSD is seldom addressed in either settings in HK and elsewhere. Meta-analyses reported the effectiveness of Internet-based cognitive behavioural therapy (iCBT), particularly when guided by therapists (d = 0.63). Personalised and synchronous instant message-based intervention guided by therapists is an emerging form of psychological intervention. While such intervention showed medium to large effect (Hedges' g = 0.73) on negative psychological distress episodes including depression, no study has investigated its effect on PSD. The proposed study aims to 1) investigate the effect of therapist-guided brief iCBT delivery through instant messaging applications (e.g. WhatsApp and WeChat) to provide personalised and synchronous PSD support and 2) understand the experience of and compliance with the intervention. 160 community-dwelling stroke survivors with Patient Health Questionnaire-9 (PHQ-9) scores ranging from 5 to 19 indicating mild to moderate depressive symptoms will be recruited and then individually randomised into the Intervention group (n=80) or Control group (n=80). Intervention group will receive 1) instant message-delivered brief iCBT for 3 months at participants' chosen times and frequencies, and 2) therapist-led text or voice message-based PSD support to enhance the effects of iCBT through real-time counselling and practical advice. Control group will only receive messages on general mental health information and reminders to participate in follow-up surveys. The primary outcome is PHQ-9 score at 6 months. Secondary outcomes will include anxiety (GAD-7), perceived stress (PSS-4), loneliness (ULS-8), and quality of life (EQ-5D-5L) at 6 months. The study will strictly follow the CONSORT-EHEALTH checklist. Post-trial qualitative study will be conducted to understand the participants' experience of and compliance with the intervention (n≈20) respectively. This study will provide the first and practical evidence on the effectiveness of instant message-delivered brief iCBT intervention in addressing PSD in HK and beyond.",[171,172,28],"Stroke","Depressive Symptoms","2024-07-10",{"date":175,"type":40},"2024-07-11",{"date":177,"type":40},"2023-05-01",{"date":179,"type":21},"2025-06",{"name":181,"class":47},"The University of Hong Kong",{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":188,"eligibilityCriteria":189,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":190,"targetDuration":4,"studyType":22,"phases":192,"briefSummary":193,"conditions":194,"keywords":196,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":200,"startDateStruct":201,"completionDateStruct":203,"leadSponsor":205,"locationsCount":206},"100508944","instant-message-delivered-early-psychological-intervention-in-stroke-family-caregivers-100508944","NCT05907005","Instant Message-delivered Early Psychological Intervention in Stroke Family Caregivers","Instant Message-delivered Early Psychological Intervention in Stroke Family Caregivers: a Mixed-method Study","EPI","Inclusion Criteria:\n\n* Primary family caregiver of first-ever stroke patient who has \\\u003C15 modified Barthel Index(mBI) scores (moderate disability);\n* Caregiver of a stroke patient who has a hospital inpatient stay of ≥6 days and ≤21days;\n* Aged ≥18;\n* Able to read and communicate in Chinese (Cantonese or Putonghua);\n* Able to use mobile phone instant messaging function; and\n* PHQ-9 (depressive symptom) score ranging from 5 to 19 (note. mild: 5-9, moderate: 10-14, moderately severe: 15-19 and severe: 20-27)\n\nExclusion Criteria:\n\n* Caregiver of stroke patient who is admitted to intensive care unit;\n* Professional medical personnel and\u002For professional carer;\n* Diagnosis of psychiatric disease before stroke event or currently taking psychotropic drug including antidepressants;\n* PHQ-9≥20 (we shall provide information on mental health services; if needed, we shall make the appropriate referrals); and\n* Currently participating in any type of psychological intervention.",{"count":191,"type":21},152,[24],"Psychological distress including depression and anxiety is a major component of caregiver stress, and its negative impact on caregivers' health and well-being has been established in the literature. A recent meta-analysis reported the prevalence of depression and anxiety in stroke caregivers as 40.2% and 21.4% respectively.\n\nAn evidence profile report by the World Health Organization(WHO) has emphasised that psychological support is crucial in helping caregivers in the community to continue caring for individuals with long-term disabilities, such as stroke patients. Therefore, early psychological intervention (EPI) is crucial to improve the management and prognosis of an individual who are facing stressful events like caregiving.\n\nThe main aim of this study is to prevent or alleviate the significant psychological consequences in carers resulting from stroke events in family members. Internet-delivered cognitive-behavioural therapy (iCBT) is delivered as an ecological momentary intervention (EMI) to support the clients to engage in cognitive reframing and empower them with proper knowledge, skills and attitudes to make behavioural changes.",[171,195,28],"Caregiver Burden",[197,198,199],"Cognitive-behavioural therapy","ecological momentary intervention","early psychological intervention",{"date":175,"type":40},{"date":202,"type":40},"2023-07-24",{"date":204,"type":21},"2025-07-31",{"name":181,"class":47},5]