How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

11,958 results for

Mobile Medical Applications

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

8361. Assessing the Impact of an Intervention to Prevent Intimate Partner Violence and HIV in Uganda

community services alone. Hypothesis 3(a): Incidence of HIV will be lower in the intervention vs. control arms. Condition or disease Intervention/treatment Phase HIV Physical Abuse of Adult (If Focus of Attention is on Victim) Sexual Abuse of Adult (If Focus of Attention is on Victim) Risk Reduction Behavior Behavioral: The SHARE Project Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 11451 participants Allocation (...) of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Intervention arm Intervention arm clusters (n=4) received an IPV prevention intervention (the Safe Homes and Respect for Everyone (SHARE) Project), enhanced HIV testing and treatment and routine HIV services. Behavioral: The SHARE Project SHARE aimed to reduce IPV and used methodologies from two proven successful violence prevention frameworks: Stepping Stones (Welbourn, 1995) and the Resource Guide

2014 Clinical Trials

8362. Short Messaging Service for Optimizing Hemoglobin A1C Management in Low-Income Diabetics

Not Applicable Detailed Description: This multi-center, unblinded, prospective randomized controlled trial will enroll adult diabetic patients of the Wilson Community Health Center, Harvest Family Health Center, and Freedom Hill Community Health Center living below 200% of 2013 poverty level with a serum hemoglobin A1C >9% and who currently own a mobile device with text messaging capacity. After written informed consent has been obtained, subjects will be randomized to intervention or control group (1:1 (...) ), stratified based on insulin initiation within 1 week of study inclusion. Participants randomized to the intervention group will be further divided into subgroups as "insulin user" or "non-insulin user" and both will receive SMS messages every 7 days. The content of the message consist of medication reminders, reporting of blood glucose results, insulin technique assessment (if applicable), or d) medication adherence assessment. Participants will be asked to respond with a simple text within 7 days

2014 Clinical Trials

8363. Study Protocol Comparing Polidocanol Versus Hypertonic Glucose for Treatment of Reticular Veins

that may be related to the study drugs any cause of dermatitis on application site free of comorbidities clinically serious as diabetes mellitus, heart failure, respiratory failure, uncontrolled hypertension with medication, and uncontrolled hypothyroidism pregnancy previous deep vein thrombosis (DVT) family history of DVT thrombophilia do not agree with the search terms Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may (...) in Treatment of Reticular Veins at the Lower Limbs. Study Start Date : September 2012 Actual Primary Completion Date : December 2014 Actual Study Completion Date : December 2014 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Polidocanol with Glucose An application session 0.2% Polidocanol + 70% Glucose to treat reticular veins of the lower limb selected, with a maximum volume of 5 ml. Drug

2014 Clinical Trials

8364. Effect of Short Message Service Intervention on Stent Removal/Exchange Adherence in Patients With Benign Pancreaticobiliary Diseases

that patients with stent implantation did not follow the recommendation of further stent management by endoscopists. Many methods have been used to improve the adherence of patients in medical service. With the advance of mobile technology and popular use of mobile phones, it was believed that the patient-centered outcome could be improved by mobile telecommunication with the timely support of a patient by a health professional. Thus we hypothesize that mobile technology, reminding the patients (...) Recruitment Status : Completed First Posted : January 22, 2014 Last Update Posted : January 22, 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: Endoscopic implantation of plastic or covered metal stents is widely used in a variety of benign pancreaticobiliary diseases, including duct stricture, large or difficult stones, bile or pancreatic juice leak, etc

2014 Clinical Trials

8365. CBT Through Internet and Smartphones for Adults With ADHD

therapy (iCBT) with an additional smartphone application and evaluated through a randomized controlled trial during 12 weeks. The patients will be randomized to one of three conditions an active treatment group where the intervention is based on cognitive - and dialectical behavioral therapy (CBT and DBT) and the mobile app. an active ICBT-treatment based on psychoeducation, a CBT stress-reduction program and Applied Relaxation, and treatment as usual (TAU) / waiting list. The main objective (...) : Internet stress-reduction Other: Treatment as usual (TAU)/waiting list Not Applicable Detailed Description: Approximately one-third of children with ADHD continue to be fully symptomatic into adulthood and many of the remainders often retain some residual problems that require treatment. Thus ADHD is a prevalent and chronic disabling disorder. Drugs provide first line treatment for adults with ADHD but are not enough for everybody, while we still lack proper evidence for promising psychological

2014 Clinical Trials

8366. Mindfulness-based Cognitive Therapy for Chronic Obstructive Pulmonary Disease

Volunteers: No Criteria Inclusion Criteria: severe to very severe COPD motivated to participate in pulmonary rehabilitation sufficient mobility to attend pulmonary rehabilitation Exclusion Criteria: certain comorbidities (e.g. unstable coronary complications, psychiatric illness) severe cognitive disability (e.g. dementia) inability to speak Danish Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study (...) (COPD) Chronic Obstructive Lung Disease Chronic Obstructive Airway Disease Chronic Bronchitis Emphysema Behavioral: Mindfulness-based cognitive therapy Behavioral: Pulmonary rehabilitation Not Applicable Detailed Description: Chronic obstructive pulmonary disease (COPD) is a major burden for the affected patients, who are continuously struggling with the hallmark symptoms breathlessness, cough, and sputum together with high levels of anxiety and depression and impairment of quality of life (QoL

2014 Clinical Trials

8367. A Clinical Study of Two Dentinal Hypersensitivity Treatments Used With Normal Oral Hygiene

Information provided by (Responsible Party): Procter and Gamble Study Details Study Description Go to Brief Summary: This study will compare the safety and effectiveness of normal oral hygiene with two different marketed dentifrices, on longer term dentinal hypersensitivity response following use of potassium oxalate desensitizers. Condition or disease Intervention/treatment Phase Dentin Sensitivity Device: Potassium oxalate Drug: Sodium fluoride paste Drug: Stannous fluoride paste Not Applicable Study (...) Completion Date : October 2014 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment oxalate liquid & gel plus SnF2 paste Potassium oxalate liquid, professionally applied Potassium oxalate gel, self applied Stannous fluoride paste, self applied Device: Potassium oxalate Professionally applied (liquid) and self applied (gel) Drug: Stannous fluoride paste Toothpaste used by subject Other Name: SnF2 paste oxalate

2014 Clinical Trials

8368. Mulligan Concept Mobilisation With Movement for Shoulder Dysfunction in Older Adults

provided by (Responsible Party): Cristina Lirio Romero, University of Alcala Study Details Study Description Go to Brief Summary: Objective: To pilot the methods proposed for conducting a full randomised clinical trial to evaluate the effect of Mulligan concept mobilization with movement on shoulder functionality in older adults with shoulder dysfunction. Design: Pilot randomised, single-blinded clinical trial. Setting: Three nursing homes, Toledo, Spain. Participants: 44 older adults with shoulder (...) -SDQ) Spanish version, and secondary outcomes are active glenohumeral range of motion and pain intensity. Data will be collected at baseline, after each group intervention, and 1 and 3 months after finishing interventions. Condition or disease Intervention/treatment Phase Disorder of Shoulder Other: Standard protocol Other: Mulligan Concept Mobilisation with Movement Not Applicable Detailed Description: Shoulder dysfunction is a common problem in older adults reaching up to 21% of prevalence

2014 Clinical Trials

8369. The Survival Rate of Glass Ionomer Cement, Glass Carbomer Cement and Compomer in Occlusal and Proximal ART Restorations

, the dentists preferred side, the child's dmft/DMFT, contamination and finally the preoperative conditions. The effect of these variables on the survival rate will be evaluated using a regression analysis. Condition or disease Intervention/treatment Phase Caries Involving Multiple Surfaces of Tooth Dental Caries on Chewing Surface of Tooth Dental Caries Extending Into Dentine Procedure: GIC Restorations Procedure: Carbomer Restorations Procedure: Compomer Restorations Not Applicable Detailed Description (...) , 2018 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: GIC Restorations Restorations using Glass Ionomer Cement Procedure: GIC Restorations Restorations using Glass Ionomer Cement Experimental: Compomer Restorations Restorations using Compomer Procedure: Compomer Restorations Restorations using Compomer Experimental: Carbomer Restorations Restorations using Glass Carbomer Procedure

2014 Clinical Trials

8370. Effects of Facility-based Mother Support Groups on Prevention of mother-to Child Transmission Outcomes in Zimbabwe

2 consists of standard of care together with facility-based MSGs. Condition or disease Intervention/treatment Phase HIV Infection Behavioral: Mother support groups for HIV+ mothers Not Applicable Detailed Description: PRIMARY OBJECTIVE To test whether MSGs lead to increased retention of HIV-exposed infants in PMTCT programmes SECONDARY OBJECTIVES To assess whether MSGs lead to increased retention of mothers in postnatal HIV follow-up care To assess whether male participation in PMTCT activities (...) will be entered, coded, cleaned and locked before analyses are made. Data will be analysed on an intention-to-treat basis. A mobile team of well-trained quality assurance and control study staff will be deployed throughout the data collection period to ensure quality of the intervention and of data generated and collected at each study site. A pre-specified proportion of patient visit records will be reviewed from each site. Study Design Go to Layout table for study information Study Type : Interventional

2014 Clinical Trials

8371. Developing a Smartphone App With Mindfulness Training for Teen Smoking Cessation

of Massachusetts Medical School Worcester, Massachusetts, United States, 01655 Sponsors and Collaborators University of Massachusetts, Worcester Investigators Layout table for investigator information Principal Investigator: Lori Pbert, PhD University of Massachusetts, Worcester Principal Investigator: Judson Brewer, MD University of Massachusetts, Worcester More Information Go to Layout table for additonal information Responsible Party: Lori Pbert, Professor of Medicine, University of Massachusetts, Worcester (...) Behavioral: Written smoking cessation materials only Not Applicable Detailed Description: The new Surgeon General's Report (SGR), Preventing Tobacco Use Among Youth and Young Adults, highlights the addictive nature of nicotine and emphasizes the need for effective and accessible cessation treatment for the more than 3.6 million youth who smoke. This proposal is in response to PA-13-078, Behavioral and Integrative Treatment Development Program (R34), which supports the development and testing

2014 Clinical Trials

8372. Abdominal Circumference and Cardiorespiratory Repercussions in Patients Submitted to Physical Therapy

chest physiotherapy. [ Time Frame: Baseline, five and thirty minutes. ] Heart rate variability has become the conventionally accepted term to describe variations of both instantaneous heart rate and intervals (time domain). Thoracoabdominal perimetry consists of a set of measurements of thoracic and abdominal circumferences during respiratory movements, and it aims at quantifying the thoracoabdominal mobility. Eligibility Criteria Go to Information from the National Library of Medicine Choosing (...) wall expansion Other: Chest physiotherapy airway clearance modality Not Applicable Detailed Description: The physiotherapist assessment will consist of anthropometry (body mass index, abdominal circumference, adipometer); chest inspection and palpation, vital signs (blood pressure, heart rate, respiratory frequence, oxymetry), dyspnea index and capillar blood glucose; and later with pulmonary tests (thoracoabdominal perimetry, respiratory muscle strength and pulmonary volume and capacity

2014 Clinical Trials

8373. Exercise in Pediatric Cancer Patient Undergoing Anti-Cancer Treatment

and balance capacity (TUDS, one leg stand), postural control functional mobility (posturomed & force plate), range of motion (goniometer) Quality of Life [ Time Frame: after primary treatment (6 month) and after one year ] KINDL questionnaire Feasibility between 6 and 12 month [ Time Frame: between end of primary treatment (6 month) and one year ] Will be measured as the proportion of patients following the exercise prescription. Eligibility Criteria Go to Information from the National Library of Medicine (...) Heidelberg Heidelberg University University of Leipzig Children`s Medical Hospital, University of Leipzig, Leipzig, Germany Information provided by (Responsible Party): German Cancer Research Center Study Details Study Description Go to Brief Summary: Today about 80% childhood cancer patients become long-time survivors. In spite of the high cure rates the diagnosis cancer is associated with a variety of disease and treatment-related psychological and physical impairments mostly present into adulthood. So

2014 Clinical Trials

8374. The Effect of Acetaminophen on Non-alcoholic Fatty Liver Disease Patients

: Presence of the metabolic syndrome, defined according to the modified AHA/NCEP criteria Taking concomitant medications Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02194894 Locations Layout table for location information United States, California (...) , and/or eosinophilia (>5%). We follow a conservative approach derived from the FDA guidelines for stopping medications expected to cause drug induced liver injury (DILI). Indeed, the FDA allows continuation of the medication until ALT or AST are >8x ULN in the absence of elevated Tbili or INR. Patients who have hepatotoxicity will have close monitoring of their liver enzymes until they normalize. Taking acetaminophen up to 3g daily has been shown to be safe and acceptable. We have followed very strict criteria

2014 Clinical Trials

8375. A Trial of Rehabilitation Therapy in Older Acute Heart Failure Patients

and 3 months ] Secondary Outcome Measures : All-Cause rehospitalization [ Time Frame: 6 months from index hospital discharge ] Other Outcome Measures: Economic Analysis [ Time Frame: 6-months ] Assess the economic impact of the intervention by comparing medical costs between treatment arms, inclusive of the cost for rehabilitation therapy, relative to its associated changes in health outcomes. Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate (...) participating in formal, facility-based cardiac rehabilitation Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02196038 Locations Layout table for location information United States, North Carolina Duke University Medical Center Recruiting Durham, North

2014 Clinical Trials

8376. Randomized Clinical Trial of Enamel Matrix Derivative: Radiographic Analysis

radiographs at baseline and after 24 months. Images were digitized and used to measure the distances from the cemento-enamel junction (CEJ) to the alveolar crest (AC), CEJ to the bottom of the defect (BD) and infrabony defect angle. Condition or disease Intervention/treatment Phase Chronic Periodontitis Drug: enamel matrix derivative Procedure: Open flap debridement Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 48 (...) ) Eligibility Criteria Go to Information from the National Library 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 and older (Adult, Older Adult) Sexes Eligible for Study

2014 Clinical Trials

8377. Hypoxia and Exercise in the Elderly

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: NCT02196623 Recruitment Status : Completed First Posted : July 22, 2014 Last Update Posted : January 24, 2019 Sponsor: Hannover Medical School Collaborator: German Diabetes Center Information provided by (Responsible Party): Hannover Medical School Study Details Study Description Go to Brief Summary: Ageing (...) is the primary risk factor for most chronic diseases including type 2 diabetes mellitus. Sarcopenia and muscular mitochondrial dysfunction with aging are crucial mechanisms leading to decreased exercise tolerance and worsened insulin sensitivity. Thus, metabolic disease and frailty, which limits physical mobility as well as quality of life, share common cellular mechanisms. The investigators will test the hypothesis that a combination of normobaric hypoxia and exercise training elicits a synergistic effect

2014 Clinical Trials

8378. Effects of Exercise on Cognitive Performance of Patients With Alzheimer-type Dementia. Pilot Study.

intensity aerobic exercise+strength Not Applicable Detailed Description: OBJECTIVE: To evaluate an intervention that combines high intensity aerobic exercise with strength (AAAD) on general cognitive performance of patients affected by mild Alzheimer's disease (AD). DESIGN: Randomized clinical trial in two parallel groups: SCOPE: 2 health center of Basque Health Service , in coordination with its reference neurology services. PARTICIPANTS: 80 patients with mild AD. INTERVENTION: Both groups receiving (...) : Global cognitive performance (Neuropsychological battery TBR-B),neuropsychiatric symptoms (NPI), ADL (Blessed),functional capacity (Test of 6-minute walk), cardiorespiratory Test, muscular strength (hand dynamometer and trunk); PREDICTORS AND CONFOUNDING VARIABLES: baseline cognitive performance, previous physical activity, medication, age, sex, APOE, schooling and cognitive reserve. ANALYSIS: We compared the two groups in terms of observed mean changes from baseline in ADAS measurement and other

2014 Clinical Trials

8379. Use of a Mechanically Passive Rehabilitation Device in Vietnam: Impact on Upper Extremity Hemiparesis After Stroke

to evaluate how stoke impacted the subject's health and life and takes 20-minutes to complete. A Vietnamese translated hard copy will be provided to the participants. A proxy version will be available in Vietnamese, in order for a caregiver or medical personnel to read the test to participants if they were unable to read or write. This survey consists of questions about physical problems, memory, mood, activities of daily living, and mobility during a 4-week timeframe (Vellone, 2014). A licensing (...) with severe to moderate stroke, but that is also simple and does not rely on powered actuators. The hypothesis is that individuals with a severe chronic stroke, who exercise with a mechanically passive rehabilitation device, will have improved arm movement ability without experiencing an increase in arm pain. Condition or disease Intervention/treatment Phase Cerebrovascular Accident Device: Resonating Arm Exerciser Not Applicable Detailed Description: A randomized control trial design will compare two

2014 Clinical Trials

8380. Pressure Sensing to Reduce the Risk of Pressure Ulcer Formation

of a pressure sensing device with continuous visual feedback of pressure imaging may potentially decrease the interface pressure of patients who are at risk of pressure ulcers in an acute hospital setting. Condition or disease Intervention/treatment Phase Pressure Ulcer Device: ForeSite PT™ system Not Applicable Detailed Description: Background: Pressure ulcers result in substantial financial costs to the healthcare system as well as significant distress to affected patients and their families. As interface (...) : Prevention Official Title: Effectiveness of a Pressure-sensing System to Reduce the Risk of Pressure Ulcer Formation by Lowering Interface Pressure in Vulnerable Patient Populations: A Parallel-two-group Randomized Controlled Trial Study Start Date : December 2014 Estimated Primary Completion Date : March 2018 Estimated Study Completion Date : March 2018 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental

2014 Clinical Trials

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>