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The effectiveness of these interventions is being examined in a series of N-of-1 trials. Each participant can choose between the interventions. After being randomly allocated to an individual sequence of one-week intervention and control phases, the study begins. Participants record their stress levels daily over the f...
Three months after the study, a survey will be sent to the participants to check if the benefits have persisted. conditions: Stress, Psychological conditions: Burnout, Psychological conditions: Subjective Stress conditions: Occupational Stress studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionMode...
<|newrecord|> nctId: NCT06368778 id: 166591 briefTitle: Real-Time Biofeedback on Partial Weightbearing Training overallStatus: ACTIVE_NOT_RECRUITING date: 2023-04-13 date: 2025-04 date: 2025-04 date: 2024-04-16 date: 2024-04-26 name: University of Utah class: OTHER briefSummary: The purpose of this study is to investig...
The primary objective of the study is to determine whether the use of the biofeedback device (Loadsol) can reduce the time it takes for healthy subjects to learn and comply with partial weightbearing, compared to traditional training methods. The Loadsol device provides real-time auditory feedback on the individual's w...
Secondary objectives of the study include:
Assessing the compliance of subjects with weightbearing restrictions in both the biofeedback and standard of care training groups, and comparing the results to identify any significant differences in adherence to the prescribed weightbearing limitations.
Evaluating subject satisfaction with the training methods, as measured through questionnaires and the use of Patient-Reported Outcomes Measurement Information System (PROMIS) tools. This evaluation will help determine if the biofeedback device (Loadsol) leads to higher levels of satisfaction among subjects compared to ...
By examining these objectives, this study aims to provide valuable insights into the potential benefits of using a biofeedback device in partial weightbearing training, and to establish whether its implementation can lead to improved outcomes in learning, compliance, and overall patient satisfaction. conditions: Physic...
<|newrecord|> nctId: NCT06368765 id: BL72 briefTitle: Oral Rehydration Solution and Dehydration Recovery overallStatus: NOT_YET_RECRUITING date: 2024-05 date: 2024-11 date: 2024-11 date: 2024-04-16 date: 2024-04-16 name: Abbott Nutrition class: INDUSTRY briefSummary: This is a prospective, randomized, controlled, blind...
<|newrecord|> nctId: NCT06368752 id: H-22063621 briefTitle: The Role of Endogenous GIP in Glycosis Metabolism During Fasting overallStatus: ENROLLING_BY_INVITATION date: 2023-05-04 date: 2023-12-12 date: 2025-12-31 date: 2024-04-16 date: 2024-04-16 name: Frederikke Koefoed-Hansen class: OTHER briefSummary: This researc...
<|newrecord|> nctId: NCT06368739 id: STUDY00005622 briefTitle: Evaluation of Medicaid Food & Nutrition Support Program for Pregnant Women overallStatus: ACTIVE_NOT_RECRUITING date: 2022-10-17 date: 2024-05-01 date: 2024-08-01 date: 2024-04-16 date: 2024-04-16 name: University of Texas at Austin class: OTHER name: Drisc...
<|newrecord|> nctId: NCT06368726 id: SFND04042024 briefTitle: Result of tDCS in ASD Children With Comorbidities Like PANDAS, Rare Genetic Diseases or Autoimmune Disorders acronym: tDCS&ASD overallStatus: ENROLLING_BY_INVITATION date: 2024-04-01 date: 2025-05-01 date: 2025-07-01 date: 2024-04-16 date: 2024-04-16 name: S...
<|newrecord|> nctId: NCT06368713 id: PD-GIEX briefTitle: Exercise Improves Gastrointestinal Function in Peritoneal Dialysis Patients overallStatus: RECRUITING date: 2024-03-01 date: 2025-06-30 date: 2025-12-31 date: 2024-04-16 date: 2024-04-16 name: Sichuan Academy of Medical Sciences class: OTHER briefSummary: This st...
<|newrecord|> nctId: NCT06368700 id: CL-00001 briefTitle: The Hyalex Early Feasibility Study (EFS) overallStatus: RECRUITING date: 2024-04-04 date: 2025-10 date: 2026-10 date: 2024-04-16 date: 2024-04-16 name: Hyalex Orthopaedics, Inc. class: INDUSTRY briefSummary: The Hyalex Early Feasibility Study is a prospective, m...
<|newrecord|> nctId: NCT06368687 id: 2023-06112-01 briefTitle: TRANPAS - TReating Anorexia Nervosa Plus Autism Spectrum acronym: TRANPAS overallStatus: NOT_YET_RECRUITING date: 2024-09-01 date: 2026-12-31 date: 2026-12-31 date: 2024-04-16 date: 2024-04-16 name: Göteborg University class: OTHER briefSummary: In a pilot ...
<|newrecord|> nctId: NCT06368674 id: 2023-00363 briefTitle: Bridging the Gap: Creating a Continuum of Care overallStatus: NOT_YET_RECRUITING date: 2024-05-02 date: 2026-12-31 date: 2027-02-01 date: 2024-04-16 date: 2024-04-22 name: Göteborg University class: OTHER name: Vastra Gotaland Region name: Narhalsan Reasearch ...
This study is relevant since today's highly specialized acute care is poorly adapted to the comprehensive needs of frail older people, and exposes them to avoidable risks such as loss of functional capacities causing unnecessary care needs and decreased wellbeing. Active follow-up by a CM after discharge may be an impo...
The intervention is a active follow-up after discharge by a CM (nurse) in primary care. CM will secure that discharge and care plans are executed and to address new needs. If there are unmet needs, the CM will ensure that adequate actions are performed to meet the needs. The intervention group consists of participants ...
<|newrecord|> nctId: NCT06368661 id: 23.79 Colo-MAR 1 briefTitle: Dietary Factors Associated to Colorectal Premalignant Lesions (COLOMAR-1) overallStatus: RECRUITING date: 2023-09-01 date: 2024-10-01 date: 2024-12-31 date: 2024-04-16 date: 2024-04-16 name: Fundación Vithas class: OTHER name: CEU San Pablo University br...
<|newrecord|> nctId: NCT06368648 id: CP-1 briefTitle: CoMind Early Feasibility Study acronym: CoMind EFS overallStatus: NOT_YET_RECRUITING date: 2024-06 date: 2025-03 date: 2025-04 date: 2024-04-16 date: 2024-04-16 name: CoMind Technologies Limited class: INDUSTRY name: Lindus Health briefSummary: The purpose of this r...
Recent research has shown it may be possible to measure ICP without needing surgery. This technology is in development, but large amounts of data is required to build these new devices.
Through collecting a large database of information from patients who have both the routine surgical device and the research device applied to their head, the research team will work to develop and test an effective and potentially safer way of monitoring patient ICP. conditions: Intracranial Pressure conditions: Intrac...
<|newrecord|> nctId: NCT06368635 id: 2022-GSP-QN-8 briefTitle: The Cerebral Microcirculation Diseases and Coronary Microcirculation Disease Study acronym: CCMD overallStatus: RECRUITING date: 2024-01-01 date: 2024-12-31 date: 2025-03-31 date: 2024-04-16 date: 2024-04-18 name: Weijing Wang class: OTHER_GOV name: Chinese...
Although a potential link between both conditions has been hypothesized based on the similarities between pathological changes and risk factors, advance in knowledge exploring this has been hampered by lacking objective evidence of CMD and pathological brain changes indicative of CSVD in prior research studies. Thus, t...
The main objective of this study was to analyse the relationship between cerebrovascular disease and CMD in patients with atherosclerotic coronary artery disease (CAD). conditions: Microcirculation conditions: Coronary Artery Disease conditions: Cerebrovascular Circulation studyType: OBSERVATIONAL observationalModel: C...
<|newrecord|> nctId: NCT06368622 id: CDM10001814 briefTitle: Evolve China PMCF Study overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2027-11 date: 2031-08 date: 2024-04-16 date: 2024-04-16 name: Stryker Neurovascular class: INDUSTRY name: Stryker (Beijing) Healthcare Products Co., Ltd briefSummary: A prospective,...
Each subject will be followed in accordance with the standard of care (SOC) at each participating hospital. conditions: Intracranial Aneurysm studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 500 type: ESTIMATED name: Surpass Evolve Flow Diverter System measure: Neurological death ...
<|newrecord|> nctId: NCT06368609 id: 2024-09 briefTitle: Preliminary Evaluation of Two Rapid Diagnostic Test Prototypes for Strongyloides Stercoralis Infection acronym: PROTOSS overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-05 date: 2024-05 date: 2024-04-16 date: 2024-04-18 name: IRCCS Sacro Cuore Don Calab...
<|newrecord|> nctId: NCT06368596 id: 2024-04 briefTitle: ENDS (ENDometriosis & FuSobacterium) Unveiling the Contribution of Fusobacterium Infection to the Development of Endometriosis acronym: ENDS overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-10 date: 2025-10 date: 2024-04-16 date: 2024-04-16 name: IRCCS ...
A control group would however be recruited for secondary objective 1 and 2.
The study is classified as interventional, as Fusobacterium detection is not part of the routine management of these patients; from the patients' point of view, participation in the study will involve the execution of additional vaginal and cervical swabs as additional procedure, while the endometrial biopsy will not r...
<|newrecord|> nctId: NCT06368583 id: 24-05 briefTitle: The Patient AS EDUcator in Anesthesia: Exploring the Patients' and Providers' Experience During Neuraxial Labour Analgesia acronym: PAS-EDU-NLA overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-12 date: 2024-12 date: 2024-04-16 date: 2024-04-23 name: Samue...
Patients who underwent labour and delivery and received labour epidural for pain management will be approached the day following the delivery, while their recollection of their experience is still fresh, and given the opportunity to participate in the study which will involve the completion of a questionnaire as well a...
<|newrecord|> nctId: NCT06368570 id: 24-04 briefTitle: The Patient AS EDUcator in Anesthesia: Exploring the Patients' Experience During Routine Cesarean Delivery acronym: PAS-EDU-RCD overallStatus: RECRUITING date: 2024-04-25 date: 2024-12 date: 2024-12 date: 2024-04-16 date: 2024-04-26 name: Samuel Lunenfeld Research ...
Patients who have undergone a routine CD will be approached the day following their delivery, while their recollection of their experience is still fresh, and given the opportunity to participate in the study, which will involve the completion of a questionnaire as well as an interview lasting approximately 20-25 minut...
<|newrecord|> nctId: NCT06368557 id: 22/59602 briefTitle: Internet-based Cognitive Behavioral Intervention for Adolescents With Anxiety Disorders overallStatus: RECRUITING date: 2023-10-10 date: 2025-03 date: 2025-06 date: 2024-04-16 date: 2024-04-16 name: Region of Southern Denmark class: OTHER name: University of Aar...
Diagnostic and Statistical Manual-5 (DSM-5) criteria. The main questions it aims to answer are:
1. If getting anxiety treatment with CoolMinds will lead to a greater reduction in anxiety symptoms, compared to a waitlist.
2. What effect different degrees of therapist support have on the treatment.
Participants will be getting 14 weeks of the iCBT intervention CoolMinds, and they will be asked to answer questionnaires about their mental health before and after the treatment.
Researchers will compare three different groups, with 56 adolescents in each group. The first group will receive iCBT with weekly scheduled feedback. The second group will get iCBT with feedback whenever the adolescents ask for it. The last group will be on a waiting list for 14 weeks, before receiving treatment. condi...
<|newrecord|> nctId: NCT06368544 id: M2023816 briefTitle: Effect of Early Gait Training on Knee Cartilage Degeneration After Anterior Cruciate Ligament Reconstruction overallStatus: RECRUITING date: 2024-01-07 date: 2030-02-07 date: 2030-02-07 date: 2024-04-16 date: 2024-04-16 name: Peking University Third Hospital cla...
<|newrecord|> nctId: NCT06368531 id: 2314270 briefTitle: Long-term Monitoring of Sleep With Ear-EEG in Patients With Chronic Pain overallStatus: RECRUITING date: 2024-04-04 date: 2025-02-15 date: 2025-08-15 date: 2024-04-16 date: 2024-04-16 name: Odense University Hospital class: OTHER name: University of Aarhus name: ...
<|newrecord|> nctId: NCT06368518 id: ID01/2024/MZHCM-Reg/NV briefTitle: Austrian HCM Registry overallStatus: RECRUITING date: 2024-03-08 date: 2034-03 date: 2034-03 date: 2024-04-16 date: 2024-04-16 name: Medical University of Graz class: OTHER briefSummary: The Austrian Hypertrophic Cardiomyopathy (HCM) Registry is a ...
<|newrecord|> nctId: NCT06368505 id: R.24.02.2506.R1 briefTitle: Platelet-Rich Plasma Injection Versus Hydrodissection in the Treatment of Carpal Tunnel Syndrome overallStatus: RECRUITING date: 2024-01-16 date: 2024-06-16 date: 2024-07-16 date: 2024-04-16 date: 2024-04-16 name: Osama Ahmed Elshafei class: OTHER briefSu...
* Which modality is more effective in reducing symptoms and improving function in patients with Carpal tunnel syndrome
* Asses safety profile of both methods
Participants will:
* Randomized to one of the two arms
* Visit the clinic 1 and 3 months after intervention
* Assessed for efficacy and safety of the intervention conditions: Carpal Tunnel Syndrome studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: DOUBLE whoMasked: PARTICIPANT whoMasked: OUTCOMES_ASSESSOR count: 64 type: ESTIMATED name: ultrasound guide...
<|newrecord|> nctId: NCT06368492 id: P137 id: 2021-002909-10 type: EUDRACT_NUMBER id: NL78008.068.21 type: OTHER domain: METC azM/Maastricht University briefTitle: The Impact of Psilocybin on Pain in Fibromyalgia Patients acronym: PsiloFM overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-12 date: 2025-12 date:...
Fibromyalgia (FM) is a chronic condition characterised by widespread pain, hyperalgesia, anxiety, disturbed sleep patterns, impaired cognitive functioning and comorbid mood disorders. Most suggested therapies are only associated with small improvements in pain ratings and quality of life. Currently, there is no data co...
Objective: The present study will explore the effects that the administration of a placebo and 2 low psilocybin doses (5 mg or 10 mg) will have on pain perception in a group of fibromyalgia patients.
Study design: The present study uses a double-blind, randomized, placebo-controlled design. All participants will receive a placebo and 2 doses of psilocybin (5 mg or 10 mg) and will undergo the Cold Pressor Test (CPT) and the Pain Pressure Threshold Task (PPT) o test its analgesic effects. conditions: Fibromyalgia stu...
<|newrecord|> nctId: NCT06368479 id: CLS-016B briefTitle: A Prospective Cross-Sectional Study to Evaluate Diagnostic Sensitivity and Specificity of iStatis HBsAg Test at the Point-Of-Care Site Settings overallStatus: RECRUITING date: 2024-03-20 date: 2024-07-01 date: 2024-07-01 date: 2024-04-16 date: 2024-04-16 name: b...
<|newrecord|> nctId: NCT06368466 id: CLS-016A briefTitle: A Prospective Cross-Sectional Study to Evaluate Diagnostic Sensitivity and Specificity of iStatis HBsAg Test at the Point-Of-Care Sites overallStatus: NOT_YET_RECRUITING date: 2024-04-30 date: 2024-08-30 date: 2024-09-01 date: 2024-04-16 date: 2024-04-16 name: b...
<|newrecord|> nctId: NCT06368453 id: CLS-003 briefTitle: A Study to Evaluate the Performance, Usability, and Result Interpretation of INSTI® HIV Self-Test overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-05-01 date: 2025-05-01 date: 2024-04-16 date: 2024-04-16 name: bioLytical Laboratories class: INDUSTRY ...
The study aims to:
To evaluate the clinical performance (i.e., diagnostic sensitivity and specificity) of the INSTI® HIV Self-Test in a lay user population.
To assess the user's comprehension of the INSTI® HIV ST results (e.g., interpreting positive, negative, and invalid results).
To evaluate the usability of the INSTI® HIV ST and understand users' experience in performing the test. conditions: Human Immunodeficiency Virus I Infection conditions: Human Immunodeficiency Virus II Infection studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: SINGLE_GROUP primaryPurpose: S...
<|newrecord|> nctId: NCT06368440 id: D7860C00003 briefTitle: A Study to Investigate the Safety and Pharmacokinetics of AZD6793 in Healthy Japanese and Chinese Participants overallStatus: NOT_YET_RECRUITING date: 2024-05-15 date: 2024-10-04 date: 2024-10-04 date: 2024-04-16 date: 2024-04-16 name: AstraZeneca class: INDU...
<|newrecord|> nctId: NCT06368427 id: D5980R00100 briefTitle: Change in Patient-repOrted Outcomes in COPD Patients Newly Initiated on TRIXEO AEROSPHERE in Real worlD acronym: COnCORD overallStatus: NOT_YET_RECRUITING date: 2024-04-30 date: 2025-09-30 date: 2025-09-30 date: 2024-04-16 date: 2024-04-16 name: AstraZeneca c...
<|newrecord|> nctId: NCT06368414 id: KCMLWP-2021-04 briefTitle: A Study of Treatment-free Remission in Chronic Phase Chronic Myeloid Leukemia acronym: AsterA overallStatus: NOT_YET_RECRUITING date: 2024-09-01 date: 2028-08-31 date: 2028-08-31 date: 2024-04-16 date: 2024-04-16 name: Korean Society of Hematology class: N...
<|newrecord|> nctId: NCT06368401 id: TP_01428 briefTitle: A First in Human Study for the Versa Device for Tricuspid Regurgitation overallStatus: NOT_YET_RECRUITING date: 2024-06-01 date: 2024-12-31 date: 2025-12-31 date: 2024-04-16 date: 2024-04-16 name: Versa Vascular, Inc class: INDUSTRY briefSummary: This study is p...
<|newrecord|> nctId: NCT06368388 id: S64854 briefTitle: Bacteriophage Therapy for Difficult-to-treat Infections: the Implementation of a Multidisciplinary Phage Task Force acronym: PHAGEFORCE overallStatus: RECRUITING date: 2021-06-01 date: 2024-12-01 date: 2025-06-01 date: 2024-04-16 date: 2024-04-16 name: Universitai...
<|newrecord|> nctId: NCT06368375 id: PRPF31-3102022BO2 briefTitle: Clinical and Genetic Findings in Patients With PRPF31-associated Retinitis Pigmentosa overallStatus: COMPLETED date: 2023-01-01 date: 2023-06-30 date: 2023-06-30 date: 2024-04-16 date: 2024-04-16 name: University Hospital Tuebingen class: OTHER briefSum...