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8441. T-116_Procera-Bridge Zirconia

Inclusion Criteria: Patients planned for treatment with a tooth-supported 3 to 4-unit bridge in any position of the maxilla or the mandible Indication: same indication as for metal supported bridges Obtained informed consent from the patient Exclusion criteria Currently known alcohol, drug or medication abuse, judged by the investigator, which might influence the follow-up program Patients where a bridge part connection area of 3 mm of diameter is not possible to obtain (short clinical crowns) Mobility (...) : The objective of the study is to evaluate the clinical performance of Procera® Bridge Zirconia veneered with NobelRondo Zirconia. Condition or disease Intervention/treatment Phase Partial Edentulism Device: Procera® Bridge Zirconia Not Applicable Detailed Description: The study was designed to be an open, 5-year, prospective, multi-center clinical post-market study. The objectives of this clinical study were that industrial centrally produced 3- or 4-unit bridges of yttrium-oxide partially-stabilized (Y-TZP

2014 Clinical Trials

8442. Fitbit One and Text Messaging Prompts to Promote Physical Activity in Overweight/Obese Adults

& Fitbit One The primary aim was to test text-messaging in its basic form to prompt physical activity. A secondary aim was to examine the effects of the Fitbit One. Other Names: Fitbit One SMS text-messaging SMS text-messages wearable sensor wearable device text message reminders text message prompts Actigraph GT3X+ self-monitoring self-regulation physical activity website tracker mobile application mobile app MVPA fairly active minutes very active minutes Active Comparator: Fitbit One Only An active (...) control group was also provided the Fitbit One to facilitate self-monitoring of PA throughout the 6-week study period. Behavioral: Fitbit One Only Active controls received a Fitbit One to facilitate self-monitoring (and no text messages) Other Names: Fitbit One wearable sensor wearable device text message reminders text message prompts Actigraph GT3X+ self-monitoring self-regulation physical activity website tracker mobile application mobile app MVPA fairly active minutes very active minutes Outcome

2014 Clinical Trials

8443. Self-Management Training and Automated Telehealth to Improve SMI Health Outcomes

service use and less acute service use costs. Condition or disease Intervention/treatment Phase Schizophrenia Schizoaffective Disorder Bipolar Disorder Depression Behavioral: CBHH+AT Behavioral: CBHH+SMT Behavioral: CBHH Not Applicable Detailed Description: Efforts to reduce early mortality in persons with serious mental illness (SMI) have largely focused on providing integrated primary care in a "health home". Yet medical care alone accounts for a disproportionately small contribution to reductions (...) a staff-to-participant ratio of approximately 1:12, with each team serving approximately 120 participants with SMI using person-centered planning and recovery-oriented, flexible service models. Each team provides mobile outreach and includes a team leader; a peer counselor; a psychiatric nurse coordinator; a clinical care coordinator; specialists in substance abuse (dual diagnosis), community integration, rehabilitation, employment, and housing; and a medical nurse practitioner (MNP) and a health

2014 Clinical Trials

8444. Nobel Procera Crown Shaded Zirconia and NobelProceraTM Full Contour Crown IPS e.Max CAD

Crown Shaded Zirconia Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 53 participants Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: A Clinical Evaluation of Hand-veneered, Porcelain-fused NobelProceraTM Crown Shaded Zirconia and NobelProceraTM Full Contour Crown IPS e.Max CAD on Molars Study Start Date : March 2010 Actual Primary Completion Date (...) : November 2013 Resource links provided by the National Library of Medicine available for: Arms and Interventions Go to Arm Intervention/treatment NobelProcera Crown Shaded Zirconia NobelProcera Crown Shaded Zirconia molar Device: NobelProcera Crown Shaded Zirconia Outcome Measures Go to Primary Outcome Measures : To compare the longevity of single cemented ceramic crowns made with shaded zirconia (NobelProceraTM Shaded Zirconia) and NobelProceraTM full contour crowns IPS e.max CAD lithium disilicate

2014 Clinical Trials

8445. Clinical Trial of a Serious Game for Individuals With SCI/D

Involvement Spina Bifida Transverse Myelitis Polio and Post-polio Syndrome Syringomyelia Spinal Stenosis Spinal Neoplasms Spinal Cord Diseases Behavioral: SCI Hard Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 184 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Prevention Official Title: Evaluating the Effectiveness of a Serious Game to Enhance (...) Self-Management Skills Among Adolescents and Young Adults With Spinal Cord Dysfunction Actual Study Start Date : February 5, 2015 Actual Primary Completion Date : September 1, 2017 Actual Study Completion Date : September 1, 2017 Resource links provided by the National Library of Medicine resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: SCI Hard This arm plays the SCI HARD game Behavioral: SCI Hard The game SCI Hard is designed to enhance self-management skills

2014 Clinical Trials

8446. Virtual Reality Rehabilitation for Individuals With Lower Limb Amputation

that can affect gait. Rheumatoid arthritis, knee joint replacement, and the use of ambulatory aids will also exclude participation. Subjects with considerable pain in their knee joints, as measured by a visual analog scale will also be excluded due to the confounding effects of pain on gait patterns. A medical history screening will be used to identify subjects with pre-existing conditions that would compromise their gait. Contacts and Locations Go to Information from the National Library of Medicine (...) by (Responsible Party): VA Office of Research and Development Study Details Study Description Go to Brief Summary: A custom designed Virtual Gait Retraining System (VGRS) is being adapted for balance and mobility rehabilitation in individuals with transtibial amputation. The system is composed of a treadmill that can simulate different environmental situations such as walking up stairs and hills and going around curves. The treadmill is synchronized with an immersive display and an avatar of the user

2014 Clinical Trials

8447. Multi-functional Neuroprosthetic System for Restoration of Motor Function in Spinal Cord Injury

: Recruiting First Posted : December 31, 2014 Last Update Posted : March 1, 2019 See Sponsor: Kevin Kilgore Collaborators: National Institute of Neurological Disorders and Stroke (NINDS) Case Western Reserve University Congressionally Directed Medical Research Programs Information provided by (Responsible Party): Kevin Kilgore, MetroHealth Medical Center Study Details Study Description Go to Brief Summary: This study is to evaluate the use of a fully implanted device for providing hand function, reach (...) , and trunk function to individuals with cervical spinal cord injury. Funding Sources: FDA OOPD NIH NINDS Condition or disease Intervention/treatment Phase Spinal Cord Injuries Device: Networked Neuroprosthetic System for Grasp and Trunk Not Applicable Detailed Description: The goal of this project is to restore these multiple functions to these individuals through a comprehensive neuroprosthetic approach that addresses the overall needs of the individual. This approach involves all aspects

2014 Clinical Trials

8448. Telementoring for Emergency Ultrasonography Performed by Emergency Physicians With Low Experience.

(resident) to manipulate the probe to get the best ultrasound image. After finishing the practice, the mentor measures the speed of used mobile network using the application of 'BENCHBEE' and records the predesigned registry. The registry includes the patients' information, the time and date of examination, the type of mobile network (3G, LTE, WiFi and etc.) and the speed of mobile network, used tele-displayer (iPhone, iPad, iPad mini), used probe, performed body organ (cardiac, lung, Hepatobiliary (...) table for study information Study Type : Observational [Patient Registry] Actual Enrollment : 103 participants Observational Model: Cohort Time Perspective: Prospective Target Follow-Up Duration: 6 Months Official Title: Telementoring for Emergency Ultrasonography Performed by Emergency Physicians Study Start Date : June 2014 Actual Primary Completion Date : December 2014 Actual Study Completion Date : April 2015 Resource links provided by the National Library of Medicine related topics: (AHRQ

2014 Clinical Trials

8449. Gait Analysis and Interdisciplinary Interventions for Children With Cerebral Palsy

interventions guided by instrumented 3-dimensional gait analysis are superior to those used in 'care as usual'. Condition or disease Intervention/treatment Phase Cerebral Palsy Other: Intervention with IGA Not Applicable Detailed Description: Children with cerebral palsy (CP) who walk independently often have an altered gait pattern. Interdisciplinary interventions in terms of orthopaedic surgery, spasticity management, physical therapy and orthotics aim to improve the gait pattern. Standardised (...) are 1) Individually tailored interdisciplinary intervention addressing impairments identified by IGA and 2) 'care as usual' (interdisciplinary interventions without IGA). The primary outcome is gait pattern measured by the Gait Deviation Index. Secondary outcome measures are, walking performance and patient-reported outcomes of functional mobility, health-related quality of life and overall health, pain and participation. Explorative outcome measures include walking performance, gait pattern

2014 Clinical Trials

8450. Outcome of Rehabilitation Following Internally Fixed Ankle Fractures

XP Walker boot Device: Plaster Immobilisation Not Applicable Detailed Description: Although the indications for fixation of an ankle fracture are relatively clear, controversy exists with regards the post-operative management of these fractures. This is a prospective randomised controlled trial. All patients admitted to the Countess of Chester NHS Foundation Trust Orthopaedic Unit for ankle fracture fixation who met the set study inclusion criteria will be given a patient information pack (...) Start Date : August 2014 Estimated Primary Completion Date : August 2016 Estimated Study Completion Date : August 2016 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment No Intervention: No Immobilisation No immobilisation post op, allowing patients to weight bear as tolerated. Active Comparator: Functional Bracing Immobilise patients in Functional brace, allowing patients to weight bear as tolerated. Device: Aircast XP

2014 Clinical Trials

8451. Evaluation of Integration Success and Crestal Bone Preservation Biomet 3i's T3 Implant System

than that of the control implant, which possess similar geometry but different surface treatments. Condition or disease Intervention/treatment Phase Partial Edentulism Tooth Disease Device: T3 with DCD tapered Prevail implant Device: Nanotite Certain tapered implant Not Applicable Detailed Description: This prospective, randomized-controlled study will enroll qualified patients with partial edentulism who will be treated with at least two dental implants. Implant sites will be randomly assigned (...) Enrollment : 100 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Investigator) Primary Purpose: Treatment Official Title: A Prospective, Randomized-controlled Evaluation of Biomet 3i's T3 Implant System for Integration Success and the Preservation of Crestal Bone Study Start Date : April 2013 Estimated Primary Completion Date : July 2017 Estimated Study Completion Date : December 2018 Resource links provided by the National Library of Medicine available

2014 Clinical Trials

8452. Comparison of Two Psycho-educational Family Group Interventions for Persons With SCI and Their Caregivers

whether participants who are more recently discharged from inpatient rehabilitation will experience greater benefit from the MFG intervention or the education control intervention. If the outcomes support the hypotheses, the MFG intervention should be made available to those with SCI and their caregivers. Condition or disease Intervention/treatment Phase Spinal Cord Injury Behavioral: Multi-Family Group Treatment Behavioral: SCI Education Control Group Not Applicable Study Design Go to Layout table (...) by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: SCI Education Control Group The SCIEC condition is a 16-session, highly structured educational intervention that provides information on how SCI affects the body; methods for maximizing function, coping, and living with SCI; and staying healthy with SCI. It also includes general guidelines for improving health behavior. Each SCIEC session follows the same structure, beginning

2014 Clinical Trials

8453. Improvement of IVF Fertilization Rates, by the Cyclic Tripeptide FEE

or disease Intervention/treatment Phase Infertility Pregnancy Other: cFFE increase the fusiogenic capacities of a gamete Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 160 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Improvement of IVF Fertilization Rates, by the Cyclic Tripeptide FEE - Prospective Randomized Study (...) of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years to 43 Years (Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patients

2014 Clinical Trials

8454. Reducing Sedentary Time in Obese Adults (Study 2)

and modify sedentary behaviors as they occur is a feasible and acceptable method of reducing sedentary time in these patients and other obese populations. Condition or disease Intervention/treatment Phase Obesity Behavioral: B-MOBILE Smartphone-Based Intervention (3-min break) Behavioral: B-MOBILE Smartphone-Based Intervention (6-min break) Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 0 participants Allocation (...) : Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: A Mobile Health Approach to Reducing Sedentary Time in Bariatric Surgery Patients Study Start Date : January 2014 Actual Primary Completion Date : December 2014 Actual Study Completion Date : December 2014 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: B-MOBILE smartphone-based

2014 Clinical Trials

8455. Effects of a Task Oriented Intervention With Two Goal-setting Approaches

would be achievable and that both groups would achieve goals that were the target of a goal-directed intervention. Condition or disease Intervention/treatment Phase Movement Disorder Learning Disability Autism Spectrum Disorder Children Behavioral: child-goal Behavioral: parent-goal Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 34 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking (...) : Single (Outcomes Assessor) Primary Purpose: Treatment Official Title: Effects of a Task Oriented Intervention for Children With Disabilities, Based on Children's or Parent's Goals, a Randomized Study. Study Start Date : October 2011 Actual Primary Completion Date : January 2014 Actual Study Completion Date : February 2014 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Child-goal The children

2014 Clinical Trials

8456. Meditation on Cognitive Function

Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 140 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: Effects of Meditation on Cognitive Function and Quality of Life Actual Study Start Date : October 2013 Estimated Primary Completion Date : October 2019 Estimated Study Completion Date : October 2020 Resource links provided (...) by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Healthy Control Group Healthy participants fill out several questionnaires asking questions about memory and concentration, mood, fatigue, how they have been feeling, and general quality of life. The questionnaires should take about 30 minutes to complete. Electroencephalography (EEG) and magnetic resonance imaging (fMRI) scan performed. These should take a total of about 90 minutes to complete

2014 Clinical Trials

8457. AUGMENTIN™ in Dental Infections

links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Amoxicillin/clavulanate Amoxicillin/ clavulanate 1 g bd for for at least 5 days upto seven days depending on treament response Drug: Amoxicillin/clavulanate Amoxicillin/clavulanate 1 g bd for at least 5 days or maximum 7 days depending upon the treatment response. Active Comparator: Clindamycin Clindamycin 150 mg qid for at least 5 days (...) in other s/sx such that no additional antimicrobial (ant) therapy is required. In event of cure or imp with complete resolution of fever and >70% reduction in swelling and pain, but 'no change' or 'worsening from BL' in other s/sx (like increased leucocyte count/tooth mobility), the inv's opinion was sought on whether additional ant therapy was required. Par. that required no additional ant therapy were considered a 'success' while those requiring additional ant therapy were deemed a 'failure

2014 Clinical Trials

8458. Lower Limb Resistance Training in Older Inpatients

' physiotherapy Outcome Measures Go to Primary Outcome Measures : Lower limb dynamometry [ Time Frame: Baseline, Week 6 ] Lower limb dynamometry will be measured using the Power Track II Commander by J-Tech Medical. A previous study in this rehabilitation unit has determined that this is a reliable measure of lower limb strength in this population. The primary outcome measurement will be quadriceps muscle strength. Secondary Outcome Measures : Functional mobility using the Timed Up and Go (TUG) [ Time Frame (...) must be able to give informed consent. Exclusion Criteria: Unstable medical condition. Patients who are unable to follow one-stage commands. Acute pain or fracture Patients who are unable to stand or require more than assistance of two staff to mobilise/transfer. Patients who have been admitted with a recent diagnosis of stroke, due to their varying patterns of recovery. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor

2014 Clinical Trials

8459. Instant Messaging Program (Wechat) Improve the Quality of Bowel Preparation

. Instant Messaging Program (Wechat) Improve the Quality of Bowel Preparation The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02140827 Recruitment Status : Completed First Posted : May 16, 2014 Last Update Posted : December 23, 2014 Sponsor: Fourth Military Medical University Information provided (...) by (Responsible Party): Yanglin Pan, Fourth Military Medical University Study Details Study Description Go to Brief Summary: Colonoscopy is the gold standard in the diagnosis of colorectal disease. The success of colonoscopy depends on high-quality bowel preparation by patients. Inadequate bowel cleansing reduces the cecal intubation rate, and the polyp detection rate (PDR). It also increases costs, mostly due to repeated procedures. The quality of bowel cleansing has remained suboptimal even though numerous

2014 Clinical Trials

8460. Cardiovascular Health in Postpartum Women Diagnosed With Excessive Gestational Weight Gain

provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: mobile health intervention Behavioral intervention. Women with excessive weight gain in pregnancy will be recruited in their 3rd trimester. They will begin with a 5 week group session on weight management. After they deliver the baby, they will begin receiving text messages supporting behavior change they learned in their 3rd trimester. They will follow up at 6 weeks (...) , not recruiting First Posted : May 20, 2014 Last Update Posted : April 20, 2016 Sponsor: Stanford University Information provided by (Responsible Party): Sandra Anping Tsai, Stanford University Study Details Study Description Go to Brief Summary: The investigators will test the efficacy of a tailored behavioral lifestyle modification program to support cardiovascular health in postpartum women with excessive gestational weight gain. This program will include a mobile health texting component postpartum

2014 Clinical Trials

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