[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07183085":3,"trial-entities:NCT07183085":90,"trial-summary:NCT07183085":94},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":21,"study_type":22,"primary_purpose":23,"phases":24,"enrollment_info":25,"interventions":28,"primary_outcomes":35,"secondary_outcomes":43,"sex":58,"minimum_age":59,"maximum_age":23,"healthy_volunteers":60,"eligibility_criteria":61,"std_ages":70,"locations":73,"central_contacts":82,"overall_officials":83,"references":88,"see_also_links":89},"NCT07183085","SH-OBS-MND-US-01","Digital Care Programs for Mental Health","Digital Care Programs for Mental Health: a Large-scale, Multi-disorder, Observational Study","ENROLLING_BY_INVITATION","2035-12","2025-09","2025-09-19","2025-09-09","Sword Health, SA","INDUSTRY",false,"The purpose of this study is to create a research repository, composed of data collected over the course of digital care programs for mental health distress delivered by Sword Mind to individuals.\n\nThis will allow the investigators to observe the acceptance, engagement, and outcomes of programs using this approach in the treatment of multiple mental health concerns.","Purpose This patient registry was designed as a research repository, composed of data collected over the course of digital care programs for mental health distress delivered by Sword Mind to individuals.\n\nThis data will allow the researchers to:\n\n1. Assess the adoption, engagement and feasibility of digital care programs for mental distress;\n2. Assess the results of digital care programs and compare the costs with the benefits obtained;\n3. Correlate the results with participant's demographic and clinical profiles;\n4. Examine the impact of mental health and the behavioral modification components of Mind's interventions on disease markers, comorbidities, and productivity;\n5. Increase the knowledge on mental distress, namely how mental health distress symptoms progress and respond to digital care programs;\n6. Develop new or improved tools to assist clinicians in the management of these disorders and in helping people achieve better mental health.\n\nDesign Prospective, observational\n\nParticipants This program is designed to support individuals experiencing mental distress to improve overall wellbeing and mood symptom improvement.\n\nParticipants will have access to a digital mental health program incorporating personalized physical and mental health exercises focused on physical activity, sleep hygiene, and mindfulness\n\nOutcomes The primary outcome will be the evolution of the participant's mental health condition along the program. Depending on the condition, primary and secondary outcome measures vary, but the registry will include, in all cases, a complete characterization of the participant's mental health status, as well as the periodic assessment of: a) performance indicators (through condition-specific tests); b) patient-reported outcomes (obtained using internationally validated pathology-specific questionnaires); c) compliance; d) patient satisfaction.",[19,20],"Mental Distress","Mental Resilience",[],"OBSERVATIONAL",null,[],{"count":26,"type":27},300000,"ESTIMATED",[29],{"type":30,"name":31,"description":32,"armGroupLabels":33},"BEHAVIORAL","Intervention","Digital mental health program incorporating personalized physical and mental health exercises focused on physical activity, sleep hygiene, and mindfulness.",[34],"Observation",[36,40],{"measure":37,"description":38,"timeFrame":39},"Anxiety","Measured through the General Anxiety Disorder-7 (GAD-7), a 7-item scale (scores 0-21). Higher scores mean higher anxiety levels.","Assessed at baseline (upon initiation of the program) and then at regular intervals (5, 9, 15, 21, and 27 days). Additional follow-up assessments may be undertaken at other follow-up times: 3 months, 6 months and 12 months.",{"measure":41,"description":42,"timeFrame":39},"Depression","Measured through the Patient Health Questionnaire-9 (PHQ-9), a 9-item scale (scores 0-27). Higher scores mean higher depression levels.",[44,48,51,54],{"measure":45,"description":46,"timeFrame":47},"Overall Improvement (PGIC)","Measured through the Patient Global Impression of Change (PGIC) questionnaire. Scores reflect the participant's perceived overall improvement (range 1-7), with higher scores indicating greater improvement.","Assessed at regular intervals (5, 9, 15, 21, and 27 days). Additional follow-up assessments may be undertaken at other follow-up times: 3 months, 6 months and 12 months.",{"measure":49,"description":50,"timeFrame":39},"Self-reported Quality of Life","Assessed through the question \"On a scale of 0-100, how would you rate your overall health, with 0 being the worst health imaginable and 100 the best health imaginable?\"",{"measure":52,"description":53,"timeFrame":39},"Work productivity and absenteeism","Measured through Work Productivity and Activity Impairment Questionnaire (WPAI) assessed by the sub-scores: WPAI overall (combining presenteeism and absenteeism), WPAI work (presenteeism), WPAI time (absenteeism) and WPAI activities (activities of daily living impairment) (scores 0-100%). Higher scores mean greater impairment.",{"measure":55,"description":56,"timeFrame":57},"Sleep Duration (wearable-measured)","Sleep will be assessed using a wearable device, including the total number of hours spent sleeping.","Recorded daily. Outcomes summarized at regular intervals (5, 9, 15, 21, and 27 days). Additional follow-up assessments may be undertaken at other follow-up times: 3 months, 6 months and 12 months.","ALL","18 Years",true,{"inclusion":62,"exclusion":65,"raw_text":69},[63,64],"18 years old and above;","able to understand study procedures and willing to provide informed consent.",[66,67,68],"suicidal ideation with plan in the past 6 months;","self-reported scores of the Patient Health questionnaire-9 (PHQ-9) above 19;","suffering from any of the following mental health conditions: Schizophrenia, Bipolar Disorder, Alcohol Use Disorder, Substance Use Disorder, Eating Disorder, Post-Traumatic Stress Disorder.","Inclusion Criteria:\n\n* 18 years old and above;\n* able to understand study procedures and willing to provide informed consent.\n\nExclusion Criteria:\n\n* suicidal ideation with plan in the past 6 months;\n* self-reported scores of the Patient Health questionnaire-9 (PHQ-9) above 19;\n* suffering from any of the following mental health conditions: Schizophrenia, Bipolar Disorder, Alcohol Use Disorder, Substance Use Disorder, Eating Disorder, Post-Traumatic Stress Disorder.",[71,72],"ADULT","OLDER_ADULT",[74],{"facility":75,"city":76,"state":76,"zip":77,"country":78,"geoPoint":79},"Sword Health","New York","10016","United States",{"lat":80,"lon":81},40.71427,-74.00597,[],[84],{"name":85,"affiliation":86,"role":87},"Fernando D Correia, MD, PhD","SWORD HEALTH INC","PRINCIPAL_INVESTIGATOR",[],[],{"nct_id":4,"conditions":91,"biomarkers":93},[92,20],"Mental distress",[],{"nct_id":4,"found":15,"summary":23,"prompt_version":23}]