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E/M Examination Criteria

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101. The cost effectiveness of m-health interventions for older adults: a systematic review

text-screening: As above, with the addition of: 7. No relevant outcome measure reported ">Prioritise the exclusion criteria Example: Two reviewers will independently extract data from each article. We first try to extract numerical data from tables, text or figures. If these are not reported, we will extract data from graphs using digital ruler software. In case data are not reported or unclear, we will attempt to contact authors by e-mail (max. 2 attempts). In case an outcome is measured (...) The cost effectiveness of m-health interventions for older adults: a systematic review Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web address: Timing

2018 PROSPERO

102. Comparing the biomechanics of brostr?m, suture anchor, and tape augmentation reconstructions for lateral ankle sprains: a systematic review

. Not about analgesics used in the clinic Full text-screening: As above, with the addition of: 7. No relevant outcome measure reported ">Prioritise the exclusion criteria Example: Two reviewers will independently extract data from each article. We first try to extract numerical data from tables, text or figures. If these are not reported, we will extract data from graphs using digital ruler software. In case data are not reported or unclear, we will attempt to contact authors by e-mail (max. 2 attempts (...) Comparing the biomechanics of brostr?m, suture anchor, and tape augmentation reconstructions for lateral ankle sprains: a systematic review Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne

2018 PROSPERO

103. Efficacy and safety of intratympanic steroid and gentamicin treatment of M?ni?re's disease: a meta-analysis

analgesics used in the clinic Full text-screening: As above, with the addition of: 7. No relevant outcome measure reported ">Prioritise the exclusion criteria Example: Two reviewers will independently extract data from each article. We first try to extract numerical data from tables, text or figures. If these are not reported, we will extract data from graphs using digital ruler software. In case data are not reported or unclear, we will attempt to contact authors by e-mail (max. 2 attempts). In case (...) Efficacy and safety of intratympanic steroid and gentamicin treatment of M?ni?re's disease: a meta-analysis Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation

2018 PROSPERO

104. A review of tailored actionable messages sent via mobile technology (m-health) to patients to promote health behaviour and manage medical conditions

A review of tailored actionable messages sent via mobile technology (m-health) to patients to promote health behaviour and manage medical conditions Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith (...) " or "Joanne") for correspondence: Organisation web address: Timing and effect measures Timing and effect measures Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web address: Context and rationale Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Example: Screening will be performed in two phases, namely initial screening

2018 PROSPERO

105. Betahistine for M?ni?re's disease or syndrome [Cochrane protocol]

: As above, with the addition of: 7. No relevant outcome measure reported ">Prioritise the exclusion criteria Example: Two reviewers will independently extract data from each article. We first try to extract numerical data from tables, text or figures. If these are not reported, we will extract data from graphs using digital ruler software. In case data are not reported or unclear, we will attempt to contact authors by e-mail (max. 2 attempts). In case an outcome is measured at multiple time points, data (...) Betahistine for M?ni?re's disease or syndrome [Cochrane protocol] Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web address: Timing and effect measures

2018 PROSPERO

106. Barriers and opportunities to implementation of sustainable e-Health programmes in Uganda: A literature review Full Text available with Trip Pro

was undertaken between May and December 2015 and was complemented with hand searching and a document review of grey literature in the form of policy documents and reports obtained online or from the Ministry of Health's Resource Centre.The searches identified a total of 293 resources of which 48 articles met the inclusion criteria of being in English and describing e-Health implementation in Uganda. These were included in the study and were examined in detail.Uganda has trialled several e-Health and m-Health (...) Barriers and opportunities to implementation of sustainable e-Health programmes in Uganda: A literature review Most developing countries, including Uganda, have embraced the use of e-Health and m-Health applications as a means to improve primary healthcare delivery and public health for their populace. In Uganda, the growth in the information and communications technology industry has benefited the rural communities and also created opportunities for new innovations, and their application

2017 African journal of primary health care & family medicine

107. Effects of Vitamin E Supplementation on Free Radicals and Fat Level of Obese Adolescence in Jakarta, Indonesia

group receiving treatment of vitamin E and other group receiving placebo. The dose and duration of vitamin E treatment is 400 IU per day for 2 months. At the end of treatment, all subjects had to run the same medical interview, physical examination and blood test. Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 69 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Quadruple (Participant, Care (...) /ml Secondary Outcome Measures : Total Cholesterol [ Time Frame: 8 weeks ] mg/dl LDL Cholesterol [ Time Frame: 8 weeks ] mg/dl HDL Cholesterol [ Time Frame: 8 weeks ] mg/dl Triglycerides [ Time Frame: 8 weeks ] mg/dl Body weight [ Time Frame: 8 weeks ] kilograms Body Height [ Time Frame: 8 weeks ] centimeters BMI [ Time Frame: 8 weeks ] kg/m^2 Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk

2017 Clinical Trials

108. The Application of the E-health Education on Shared Care Program for Patients With Type 2 Diabetes

. Recruitment status was: Recruiting First Posted : February 23, 2017 Last Update Posted : February 23, 2017 Sponsor: Li-Li Chen Information provided by (Responsible Party): Li-Li Chen, China Medical University Hospital Study Details Study Description Go to Brief Summary: This study will be a randomized controlled trial aimed at examining the effectiveness of the in e-health education on shared care program for patients with type 2 diabetes mellitus (T2DM). The experiment will be conducted over 1 year (...) will be measured at three time points including 1 month before the experiment, and 2 and 5 months after the experiment. The self-management conditions and quality of life of the subjects will be also recorded using relevant scales. Condition or disease Intervention/treatment Phase Type 2 Diabetes Mellitus Behavioral: E-health Education Other: Routine care Not Applicable Detailed Description: This study will be a randomized controlled trial aimed at examining the effectiveness of the in e-health education

2017 Clinical Trials

109. Effects of Ecological Rythmic-acoustic Stimulation (E-RAS) on Motor Skills in Individuals With Parkinson's Disease

of the auditory cues; absence of significant cognitive impairment (i.e., Mini-Mental Status Examination (MMSE) > 24; Frontal Assessment Battery (FAB) > 13); absence of psychiatric or severe systemic illnesses; mild-to-moderate disability assessed by means of the modified Hoehn and Yahr (H&Y) staging scale (1,5 ≤ H&Y ≤ 3); no engagement in any rehabilitative program in the 3 months before the beginning of the study Exclusion Criteria: Contacts and Locations Go to Information from the National Library (...) Effects of Ecological Rythmic-acoustic Stimulation (E-RAS) on Motor Skills in Individuals With Parkinson's Disease Effects of Ecological Rythmic-acoustic Stimulation (E-RAS) on Motor Skills in Individuals With Parkinson's Disease - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number

2017 Clinical Trials

110. Ultrasound - Performing Diagnostic Obstetric Ultrasound Examinations

Ultrasound Examinations 2 TABLE OF CONTENTS I. INTRODUCTION 3 II. SONOLOGIST'S CREDENTIALS CRITERIA 3 III. SONOGRAPHER'S CREDENTIALS CRITERIA 3 IV. DOCUMENTATION 3 V. SUPERVISION AND INTERPRETATION OF ULTRASOUND EXAMINATIONS 4 VI. QUALITY IMPROVEMENT PROGRAMS 4 VII. EQUIPMENT 4 VIII. TYPES OF FETAL SONOGRAPHIC EXAMINATIONS 4 IX. SONOGRAPHIC TECHNIQUE 5 A. First Trimester Sonography 5 B. Second and Third Trimester Sonography 5 C. Limited Examination 8 D. Specialized Examination 8 X. FETAL SAFETY 8 (...) of the umbilical vein and portal sinus, and which should include the fetal stomach. e. Fetal growth and weight (as opposed to gestational age) should be assessed in the late second and third trimesters. Abdominal circumference measurement is necessary along with other biometric parameters to estimate fetal weight and may allow detection of intrauterine growth restriction and macrosomia. Canadian Association of Radiologists CAR Standard for Performing Diagnostic Obstetric Ultrasound Examinations 7 If previous

2010 Canadian Association of Radiologists

111. Criteria for appropriate use of FDG-PET in breast cancer

of confidence in the overall evidence for each outcome of interest. The GRADE approach for diagnostic recommendations was also used to elicit judgement from the panel members on benefit and harms trade-off for patient-important outcomes. The RAND method was used to vote and reach an agreement on the appropriateness criteria. Results: The panel examined and assessed the role of FDG-PET for the following 7 clinical indications: Diagnosis of primary breast cancer; N staging of primary breast cancer; M staging (...) , Longo G. Criteria for appropriate use of FDG-PET in breast cancer . Bologna: Agenzia sanitaria e sociale regionale, Regione Emilia-Romagna (ASSR). ORIentamenti 3. 2011 Authors' conclusions Aim: The criteria reported in this document, are to be intended as guidance for programs of clinical governance aimed at: supporting clinicians on the use of FDG-PET; post hoc analyses of appropriate use of FDG-PET; contributing to the planning of the regional health service. Method: A panel of 23 experts

2011 Health Technology Assessment (HTA) Database.

112. Criteria for appropriate use of FDG-PET in esophageal cancer

in the overall evidence for each outcome of interest. The GRADE approach for diagnostic recommendations was also used to elicit judgement from the panel members on benefit and harms trade-off for patient-important outcomes. The RAND method was used to vote and reach an agreement on the appropriateness criteria. Results: The panel examined and assessed the role of FDG-PET for the following 7 clinical indications: N staging of primary esophageal cancer; M staging of primary esophageal cancer; Target volume (...) . Criteria for appropriate use of FDG-PET in esophageal cancer. Bologna: Agenzia sanitaria e sociale regionale, Regione Emilia-Romagna (ASSR). ORIentamenti 4. 2011 Authors' conclusions Aim: The criteria reported in this document, are to be intended as guidance for programs of clinical governance aimed at: supporting clinicians on the use of FDG-PET; post hoc analyses of appropriate use of FDG-PET; contributing to the planning of the regional health service. Method: A panel of 26 experts, comprising

2011 Health Technology Assessment (HTA) Database.

113. Criteria for appropriate use of FDG-PET in colorectal cancer

in the overall evidence for each outcome of interest. The GRADE approach for diagnostic recommendations was also used to elicit judgement from the panel members on benefit and harms trade-off for patient-important outcomes. The RAND method was used to vote and reach an agreement on the appropriateness criteria. Results: The panel examined and assessed the role of FDG-PET for the following 7 clinical indications: N staging of primary esophageal cancer; M staging of primary esophageal cancer; Target volume (...) . Criteria for appropriate use of FDG-PET in colorectal cancer . Bologna: Agenzia sanitaria e sociale regionale, Regione Emilia-Romagna (ASSR). ORIentamenti 5. 2011 Authors' conclusions Aim: The criteria reported in this document, are to be intended as guidance for programs of clinical governance aimed at: supporting clinicians on the use of FDG-PET; post hoc analyses of appropriate use of FDG-PET; contributing to the planning of the regional health service. Method: A panel of 26 experts, comprising

2011 Health Technology Assessment (HTA) Database.

114. The accuracy of NDO-LID antigen based ELISA assay relative to PGL-1 antigen for antibodies detection against M. leprae in leprosy patients: a systematic review protocol

The accuracy of NDO-LID antigen based ELISA assay relative to PGL-1 antigen for antibodies detection against M. leprae in leprosy patients: a systematic review protocol Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (...) (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web address: Timing and effect measures Timing and effect measures Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web address: Context and rationale Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Inclusion criteria: Exclusion criteria: Example: Screening will be performed in two phases, namely

2017 PROSPERO

115. PROMs for pain in adult cancer patients and use of m-health: a systematic review of measurement properties

analgesics used in the clinic Full text-screening: As above, with the addition of: 7. No relevant outcome measure reported ">Prioritise the exclusion criteria Example: Two reviewers will independently extract data from each article. We first try to extract numerical data from tables, text or figures. If these are not reported, we will extract data from graphs using digital ruler software. In case data are not reported or unclear, we will attempt to contact authors by e-mail (max. 2 attempts). In case (...) PROMs for pain in adult cancer patients and use of m-health: a systematic review of measurement properties Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation

2017 PROSPERO

116. Impact of the Radiographic Examination on Diagnosis and Treatment Decision of Caries Lesions in Primary Teeth

-000 Sponsors and Collaborators University of Sao Paulo Conselho Nacional de Desenvolvimento Científico e Tecnológico Fundação de Amparo à Pesquisa do Estado de São Paulo Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. Investigators Layout table for investigator information Principal Investigator: Fausto M Mendes, PhD School of Dentistry, University of Sao Paulo More Information Go to Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number): Layout (...) Impact of the Radiographic Examination on Diagnosis and Treatment Decision of Caries Lesions in Primary Teeth Impact of the Radiographic Examination on Diagnosis and Treatment Decision of Caries Lesions in Primary Teeth - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies

2014 Clinical Trials

117. Examining Tolerance to CNS Stimulants in ADHD

International University Investigators Layout table for investigator information Principal Investigator: William E Pelham, Ph.D. Florida International University Principal Investigator: James M Swanson, Ph.D. Florida International University More Information Go to Additional Information: Layout table for additonal information Responsible Party: Florida International University ClinicalTrials.gov Identifier: Other Study ID Numbers: MH099030 First Posted: January 20, 2014 Last Update Posted: July 9, 2018 Last (...) Examining Tolerance to CNS Stimulants in ADHD Examining Tolerance to CNS Stimulants in ADHD - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Examining Tolerance to CNS Stimulants in ADHD The safety

2013 Clinical Trials

118. Acute Cardiorespiratory Effects of E-cigarette Inhalation

examination Normal EKG Normal blood tests Normal lung function Exclusion Criteria: Cardiovascular disease Respiratory disease Systemic or chronic disorders or disease Symptoms of infection or inflammation within 2 weeks of the study BMI≥30 Pregnancy Current habitual cigarette smokers 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 (...) Acute Cardiorespiratory Effects of E-cigarette Inhalation Acute Cardiorespiratory Effects of E-cigarette Inhalation - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Acute Cardiorespiratory Effects of E

2016 Clinical Trials

119. Motivational Instant Messaging and E-diabetes Prevention Programme for High Risk of Type 2 Diabetes

/treatment Phase Pre-diabetes Device: Wearable technology Behavioral: Diabetes Prevention Programme educational material Behavioral: Motivational messaging Not Applicable Detailed Description: The study will examine whether a wearable technology, combined with biofeedback, motivational messaging and an e-diabetes prevention programme, is effective in reducing weight and increasing physical activity after 12 months. The intervention will consist of a wearable technology and a smartphone application made (...) Criteria: HbA1c between 42 and 47 mmol/mol BMI≥25 kg/m² Fluent in conversational English Permanent resident in Lambeth, Southwark or Lewisham Ownership of a smartphone (iPhone or Android only) for communication defined as logging on at least once/day to the internet Ambulatory. Exclusion Criteria: Known diabetes Pregnancy or planning pregnancy during the duration of the study Severe mental illness (severe depression, psychosis, bipolar affective disorder, dementia, learning difficulties, substance

2016 Clinical Trials

120. E. Coli Nissle 1917

E. Coli Nissle 1917 E. Coli Nissle 1917 - Suspension for Infection Prophylaxis - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. E. Coli Nissle 1917 - Suspension for Infection Prophylaxis (RONi) The safety (...) Summary: This study evaluates the long term effects of E. coli strain Nissle 1917 (EcN-Suspension) probiotic bacteria administration on the number of both, bacterial and viral infections during the first 24 months of infant's life. Half of study participants will receive EcN-Suspension, while the other half will receive placebo. In an additional non-clinical explorative evaluation will furthermore be investigated whether the early intestinal colonization with E.coli strain Nissle 1917 affects

2016 Clinical Trials

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