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.

11,921 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

8381. Fibers and Gut Health

-morbid illnesses such as cardiovascular, endocrine, renal or other chronic disease likely to affect gut motility or limit normal functions (e.g. reduced mobility or increased fragility) Ongoing alcohol, drug, or medication abuse (anamnesis only) Self-reported symptoms of pelvic organ prolapse Moderate or severe active local anorectal problems such as recurrent anal fissures, bleeding, large prolapsing haemorrhoids Regular use of fiber supplementation (e.g. Fybogel, Lactulose) (i.e. no more than 1 (...) in adults with functional constipation. Condition or disease Intervention/treatment Phase Constipation Other: High quantity fiber Other: Low quantity fiber Other: Placebo Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 120 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) Primary Purpose: Prevention Official

2014 Clinical Trials

8382. Is Patients With Pulmonary Disease Benefit a Program With Yogic Exercises?

on the 6MWT Acute dyspnea Surgery within 6 months Medication affecting attention, sudden change of medication. 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): NCT02233114 Locations Layout table for location information Sweden Karolinska University hospital (...) ): Per Wandell, Karolinska Institutet Study Details Study Description Go to Brief Summary: Is Yogic Exercises (12 weeks) increasing respiratory function, functional capacity and quality of life in patients with obstructive lung diseases. With follow up after 6 months. Condition or disease Intervention/treatment Phase COPD Asthma Other: Yogic exercises Other: Physiotherapy Not Applicable Detailed Description: Is Yogic Exercises increasing respiratory function in patients with obstructive lung diseases

2014 Clinical Trials

8383. Diaphragm Release Manual Technique Efficacy in COPD Patients

release technique (sham) Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 26 participants Allocation: Randomized Intervention Model: Single Group Assignment Masking: Double (Participant, Outcomes Assessor) Primary Purpose: Treatment Official Title: Diaphragm Release Manual Technique Efficacy on Diaphragmatic Mobility, Respiratory Muscle Strength and Exercise Performance in COPD Patients: a Randomized Controlled Trial (...) by (Responsible Party): Helga Cecília Muniz de Souza, Universidade Federal de Pernambuco Study Details Study Description Go to Brief Summary: The aims of this study are to evaluate the effects of Diaphragm Release Manual Technique on diaphragm mobility, chest wall kinematics and functional capacity of COPD patients. Methods: Randomized controlled trial (double blinded) with COPD patients, allocated in two group: intervention (IG) who will receive the Diaphragm Release manual technique on 6 non-consecutive

2014 Clinical Trials

8384. Pain Relief After Colorectal Surgery: Spinal Combined With Painbuster® vs Painbuster® Alone.

: 24 hours ] Peripheral blood samples taken at baseline, 60 minutes after surgical incision and 24 hours postoperatively will be analysed for cortisol and noradrenaline. Secondary Outcome Measures : Length of hospital stay or fitness for discharge [ Time Frame: Up to 12 days ] Discharge criteria: Good pain control with oral analgesia. Tolerating solid food without nausea and vomiting. No IV fluid or medication. Independently mobile and self-caring or at the same level as prior to admission. Stable (...) or disease Intervention/treatment Phase Colorectal Cancer Procedure: Spinal and infusion of local anaesthetic Procedure: Continuous infusion of local anaesthetic Drug: Bupivacaine Drug: Diamorphine Device: A Painbuster® catheter Device: 25G Whitacre needle Not Applicable Detailed Description: This is a pilot randomised controlled trial Hypotheses - Following colorectal surgery, spinal anaesthesia combined with a continuous infusion of local anaesthetic into the surgical wound provides better pain relief

2014 Clinical Trials

8385. Pilates, Postural Global Reeducation and Ball Exercises

movement in the test distance of the third finger to the ground Exclusion Criteria: Individuals with excessive absences (more than 20% of sessions) or those who missed and could not reset the session in the same week were excluded -Individuals who needed to undergo some surgery or any medical treatment during the duration of the study, or those who give up without completing the minimum time of the intervention Contacts and Locations Go to Information from the National Library of Medicine To learn more (...) Details Study Description Go to Brief Summary: The purpose of this study is to evaluate and compare the effects of three Exercise Movement Techniques Global Postural Reeducation(RPG), Pilates method and Segmented Dynamic Exercises (SDE) regarding muscular strength and endurance of the trunk, spine mobility and flexibility of the posterior muscle chain. Condition or disease Intervention/treatment Phase Strength, Muscle Endurance , Physical Flexibility Other: Pilates Group Other: Segmented Dynamic

2014 Clinical Trials

8386. Effectiveness of Two Water-Based Potassium Oxalate Desensitizers

: Double (Participant, Investigator) Primary Purpose: Treatment Study Start Date : July 2014 Actual Primary Completion Date : September 2014 Actual Study Completion Date : September 2014 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: potassium oxalate gel Professional application Device: Potassium oxalate Other Name: Professional application Active Comparator: Potassium oxalate liquid (...) Professional application Device: Potassium oxalate Other Name: Professional application Outcome Measures Go to Primary Outcome Measures : Dentin sensitivity [ Time Frame: 30 days ] Schiff Index Secondary Outcome Measures : Dentin sensitivity [ Time Frame: 30 Days ] Visual Analog Scale 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

2014 Clinical Trials

8387. Physiotherapy in Hematopoietic Stem Cell Transplantation

) ] Medical diagnosis, age (years), height (cm), weight (kg) 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 (...) underwent a physiotherapy treatment that takes place during the pre-and post-transplant period, compared to a control group. Condition or disease Intervention/treatment Phase Hematologic Malignancy Stem Cell Transplantation Other: Physiotherapy in patients with stem cell transplantation Not Applicable Detailed Description: The main characteristics of the study are: Randomized, prospective and longitudinal in patients receiving allogeneic hematopoietic stem cell transplantation clinical trial

2014 Clinical Trials

8388. Study of Efficacy and Safety of CTL019 in Pediatric ALL Patients

by morphologic assessment at screening Life expectancy > 12 weeks Age 3 at the time of screening per protocol to age 21 at the time of initial diagnosis Karnofsky (age ≥ 16 years) or Lansky (age < 16 years) performance status ≥ 50 at screening Signed written informed consent and assent forms (if applicable) must be obtained prior to any study procedures Once all other eligibility criteria are confirmed, must have an apheresis product of non-mobilized cells received and accepted by the manufacturing site (...) Leukemia Actual Study Start Date : August 14, 2014 Actual Primary Completion Date : May 29, 2018 Estimated Study Completion Date : December 5, 2022 Resource links provided by the National Library of Medicine related topics: available for: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: CTL019 Pediatric patients with relapsed/refractory B-cell ALL Biological: CTL019 T-cells A target dose of CTL019 transduced cells will consist of a single infusion of 2.0 to 5.0 x 10^6

2014 Clinical Trials

8389. Liposomal Bupivacaine Versus Standard of Care in Total Knee Surgery

Party): Robert Fada, MD, OhioHealth Study Details Study Description Go to Brief Summary: The purpose of this study is to determine whether liposomal bupivacaine is effective in the management of pain following total knee arthroplasty, as compared to standard of care analgesia. Condition or disease Intervention/treatment Phase Osteoarthritis, Knee Drug: Liposomal bupivacaine Drug: Standard of Care Not Applicable Detailed Description: Liposomal bupivacaine (Exparel®) is a local anesthetic made up (...) arthroplasty. This has the potential to avoid the need for opioid medications. With better pain control, medication side effects can be avoided and patient's length of stay in the hospital can be shortened. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 60 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Participant) Primary Purpose: Treatment Official Title: Local Liposomal Bupivacaine

2014 Clinical Trials

8390. Smoking Response Inhibition Training

): North Dakota State University Study Details Study Description Go to Brief Summary: The current study tests a response inhibition retraining program, implemented on a mobile device, as a mechanism to increase relapse prevention during a smoking cessation attempt. Study participants (n = 150) are randomly assigned to a control, benign, or intervention condition. They complete 2 weeks of response inhibition retraining, and then engage in a cessation attempt. It is hypothesized that individuals who (...) receive the intervention will have a decreased likelihood of relapse following the cessation attempt. In addition, it is hypothesized that this is due to decreases in implicit smoking motivation as a function of the response inhibition training. Condition or disease Intervention/treatment Phase Smoking Cessation Behavioral: Response Inhibition Training Not Applicable Detailed Description: Smoking is the leading preventable cause of death and disease in the U.S. Each year approximately 30% of smokers

2014 Clinical Trials

8391. NobelProceraTM Bridge Shaded Zirconia

- or 4-unit bridges of shaded yttrium-oxide partially-stabilized (Y-TZP) zirconia (NobelProceraTM Shaded Zirconia) in combination with a veneering ceramic material will show sufficient CDA ratings and a sufficient survival rate after 5 years Condition or disease Intervention/treatment Phase Posterior Bridge Restoration Device: NobelProcera Bridge Shaded Zirconia Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 25 (...) participants Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: A Clinical Evaluation of NobelProceraTM Bridge Shaded Zirconia Actual Study Start Date : June 18, 2010 Actual Primary Completion Date : November 23, 2013 Actual Study Completion Date : November 23, 2013 Resource links provided by the National Library of Medicine available for: Arms and Interventions Go to Arm Intervention/treatment NobelProcera Bridge Shaded Zirconia posterior

2014 Clinical Trials

8392. Cardiovascular Response to Two Manual Techniques for Neck Pain

: Anterior to posterior pressures Procedure: Lateral glide Not Applicable Detailed Description: To be included in the study, these subjects with unilateral non-traumatic, non-chronic neck pain (operationally defined as neck pain with mobility deficits lasting less than 3 months) shall have numeric pain rating scale (NPRS) of between 0 and 5 out of 10 as the most painful neck movement even with passive scapular elevation, neck disability index (NDI) of between 16 and 50 out of 100%, resting systolic (...) Resting heart rate between 60 and 90 beats per minute Exclusion Criteria: Current smoker Under 18 years and over 50 years of age History of fainting spells or loss of consciousness Currently on blood thinners Taking medications for or have a history of diabetes mellitus, neurologic or cardiovascular disease History of spinal surgery Has neck pain classified or associated headache, arm pain, trauma/whiplash Contacts and Locations Go to Information from the National Library of Medicine To learn more

2014 Clinical Trials

8393. The Medacta International GMK Sphere Post-Marketing Surveillance Study

cannot or will not provide informed consent for participation in the study Those whose prospects for a recovery to independent mobility would be compromised by known coexistent, medical problems Patient whose BMI exceeds 40 Any case not described in the inclusion criteria 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 (...) : Medacta International SA Information provided by (Responsible Party): Medacta International SA Study Details Study Description Go to Brief Summary: This is a Post-Marketing Surveillance of GMK Sphere knee prosthesis. Condition or disease Intervention/treatment Phase Arthritis Traumatic Arthritis Rheumatoid Arthritis Poly-arthritis Avascular Necrosis Device: GMK Sphere Knee Replacement Not Applicable Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial

2014 Clinical Trials

8394. Open Reduction Syndesmosis Tightrope Versus Screw Fixation

screw fixation in a randomized controlled trial. In this multi centre randomized study, radiographic, economic and functional outcomes are compared between [open reduction, flexible Tightrope syndesmosis fixation (OT)] and [open reduction screw fixation (OS)] of the syndesmosis. Condition or disease Intervention/treatment Phase Ankle Fractures Device: Open reduction Tightrope fixation Device: open reduction screw fixation Not Applicable Detailed Description: Tibia-fibular syndesmosis injury occurs (...) Intervention Model: Single Group Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: A Prospective Randomized Multi Center Study to Compare Open Reduction, TightRope Fixation (OT) Versus Open Reduction Screw Fixation (OS) of the Tibia - Fibular Syndesmosis. Actual Study Start Date : April 2015 Actual Primary Completion Date : September 2017 Actual Study Completion Date : September 2017 Resource links provided by the National Library of Medicine related topics: Arms

2014 Clinical Trials

8395. Physiotherapy in the Haemophilic Arthropathy of the Elbow.

and arthropathy of the elbow. Condition or disease Intervention/treatment Phase Patients With Hemophilia Other: Manual Therapy Other: Educational group Not Applicable Detailed Description: The intervention was carried out during twelve weeks, performing evaluations before and after treatment, and six months of finalizing this. The treatment of MT group consisted of two sessions per week, one hour each, and the treatment of group E consisted in a session for 90 minutes every two weeks, with daily home (...) Actual Primary Completion Date : October 2012 Actual Study Completion Date : June 2014 Resource links provided by the National Library of Medicine related topics: related topics: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: Manual Therapy group The treatment of this group consisted of two sessions per week, one hour each. We used joint traction, passive muscles stretching and Proprioceptive Neuromuscular Facilitation Other: Manual Therapy 5 minutes. Termotherapy

2014 Clinical Trials

8396. Manual Therapy in Haemophilic Arthropathy of the Knee

Intervention/treatment Phase Patients With Haemophilia Other: Manual Therapy Other: Educational Physiotherapy Not Applicable Detailed Description: Randomized trial with two treatment groups: one using joint traction, passive muscle stretching and isometric exercises, active resisted and proprioception exercises (group MT); and another with educational sessions and home exercises (group E); and a control group (group C). The intervention was carried out during twelve weeks, performing evaluation before (...) of Medicine related topics: related topics: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: Manual Therapy group We employed joint traction, passive muscle stretching and isometric exercises, active resisted and proprioception exercises. The treatment in this group consisted of two sessions per week for one hour each. Other: Manual Therapy 5 minutes. Thermotherapy shallow to 50 cm away from the knee. 15 minutes. Joint traction, grade I-II. Fixation of distal femur

2014 Clinical Trials

8397. Short-term Outcomes of Iridoplasty for Persistent Angle Closure Despite Patent Iridotomies

meridians at the same room illumination of 14 lux measured with a luxometer mobile application (Apple Inc., Application Manufactory available at the AppStore by June 2012). Images were analyzed in a masked manner marking scleral spurs and angle recess at 0° and 180° of the horizontal image. ALPI was applied with a VISULAS diode laser of 532 nm (Carl Zeiss Meditec, Dublin, CA) by the same ophthalmologist (JML). Twenty to 40 spots of 400 mW power with 500 microns of size and duration of 500 ms were (...) vault) at 0° and 180° as the main outcome measure to determine effectiveness. Condition or disease Intervention/treatment Phase Angle Closure Glaucoma Glaucoma Procedure: Argon Laser Peripheral Iridoplasty Not Applicable Detailed Description: Background Argon laser peripheral iridoplasty (ALPI) (Figure 1) is an iris-remodeling procedure that intends to widen the iridocorneal angle through redistribution of peripheral iris tension forces close to the trabeculum. ALPI is effective in patients

2014 Clinical Trials

8398. Lateral Cord Stimulation as a New Treatment for Refractory Spastic Cerebral Palsy

in selected cases of patients with cerebral palsy Condition or disease Intervention/treatment Phase Cerebral Palsy Spasticity Device: Lateral spinal cord surgical implant of electrodes Not Applicable Detailed Description: PROJECT Lateral Cord Stimulation was thought by the author to be employed in patients with spastic cerebral palsy with the aim to improve tonus, motor function and speech. Nevertheless, as it has been demonstrated as acting on the basic phenomena related with spasticity, it's to say (...) : None (Open Label) Primary Purpose: Treatment Official Title: Lateral Cord Electrical Stimulation Can Improve Spasticity in Chronic Spastic Cerebral Palsy Estimated Study Start Date : December 1, 2019 Estimated Primary Completion Date : December 2020 Estimated Study Completion Date : March 2022 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Spasticity, Cerebral Palsy To perform a Lateral spinal cord

2014 Clinical Trials

8399. Exercise, Brain Imaging, Cognition, and Gait in Parkinsonism

and Science University Collaborator: National Institute on Aging (NIA) Information provided by (Responsible Party): Fay B. Horak, Oregon Health and Science University Study Details Study Description Go to Brief Summary: There is emerging research detailing the relationship between balance/gait/falls and cognition. Imaging studies also suggest a link between structural and functional changes in the frontal lobe (a region commonly associated with cognitive function) and mobility. People with Parkinson's (...) disease have important changes in cognitive function that may impact rehabilitation efficacy. Our underlying hypothesis is that cognitive function and frontal lobe connections with the basal ganglia and brainstem posture/locomotor centers are responsible for postural deficits in people with Parkinson's disease and play a role in rehabilitation efficacy. The purpose of this study is to 1) determine if people with Parkinson's disease can improve mobility and/or cognition after partaking in a cognitively

2014 Clinical Trials

8400. Prehospital Stroke Study at the Universitair Ziekenhuis Brussel I (PreSSUB I)

as an interaction between the patient in the ambulance and a remote teleconsultant, that results in a medical intervention and/or timely communication of medically relevant information to the inhospital team. 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 (...) Age >= 18 years Suspicion of acute stroke with symptom onset <12 h or unknown, based on any of the symptoms mentioned in the Belgian manual for medical regulation of pre-hospital care: Hemiparesis, Facial asymmetry, Speech disturbance, Sudden, severe headache, or Confusion. Exclusion Criteria: Patients for whom telemedicine consultation would delay any diagnostic or therapeutic intervention. Contacts and Locations Go to Information from the National Library of Medicine To learn more about

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 >>>>