Electronic Medical Records (EMR) Clinical Trials This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.

A Study of Channeling in the Use of Nonprescription Paracetamol and Ibuprofen in an Electronic Medical Records Database: Evidence and Implications
 Conditions : Hemorrhage, Gastrointestinal; Myocardial Infarction; Stroke; Kidney Diseases Intervention : Sponsor : Janssen Research & Development, LLC Active, not recruiting - verified July 2016 (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - June 7, 2016 Category: Research Source Type: clinical trials

A Study of Channeling in the Use of Nonprescription Paracetamol and Ibuprofen in an Electronic Medical Records Database: Evidence and Implications
Conditions: Hemorrhage, Gastrointestinal; Myocardial Infarction; Stroke; Kidney DiseasesIntervention: Sponsor: Janssen Research & Development, LLCActive, not recruiting - verified July 2016 (Source: ClinicalTrials.gov)
Source: ClinicalTrials.gov - June 7, 2016 Category: Research Source Type: clinical trials

Yoga versus education for Veterans with chronic low back pain: study protocol for a randomized controlled trial
This study is a parallel randomized controlled trial comparing yoga to education for 120 Veterans with chronic low back pain. Participants are Veterans ≥18 years old with low back pain present on at least half the days in the past six months and a self-reported average pain intensity in the previous week of ≥4 on a 0–10 scale. The 24-week study has an initial 12-week intervention period, where participants are randomized equally into (1) a standardized weekly group yoga class with home practice or (2) education delivered with a self-care book. Primary outcome measures are change at 12 weeks in low back pain in...
Source: Trials - April 28, 2016 Category: Research Source Type: clinical trials

Choice of Moisturiser for Eczema Treatment (COMET): study protocol for a randomized controlled trial
Discussion Recruitment is on-going. At the end of the study, as well as being able to answer the question, ‘Is it is possible to recruit and retain children with eczema from primary care into a four-arm randomized trial of emollients?’, we will also have collected important data on the acceptability and effectiveness of four commonly used emollients. Trial registration Current Controlled Trials ISRCTN21828118 and Clinical Trials Register EudraCT2013-003001-26. (Source: Trials)
Source: Trials - July 15, 2015 Category: Research Source Type: clinical trials

What is the effect of a formalised trauma tertiary survey procedure on missed injury rates in multi-trauma patients? Study protocol for a randomised controlled trial
Discussion The findings of this study may alter the delivery of international trauma care. If formal TTS is (cost-) effective this intervention should be implemented widely. If not, where already partly implemented, it should be abandoned. Study findings will be disseminated widely to relevant clinicians and health funders. Trial registration ANZCTR: ACTRN12613001218785, prospectively registered, 5 November 2013 (Source: Trials)
Source: Trials - May 13, 2015 Category: Research Source Type: clinical trials

Do clinical decision-support reminders for medical providers improve isoniazid preventative therapy prescription rates among HIV-positive adults?: study protocol for a randomized controlled trial
This study will examine the use of clinical decision-support reminders to improve rates of initiation of preventative treatment in a TB/HIV co-morbid population living in a TB endemic area. This will be a pragmatic, parallel-group, cluster-randomized superiority trial with a 1:1 allocation to treatment ratio. For the trial, 20 public medical facilities that use clinical summary sheets generated from an electronic medical records system will participate as clusters. All HIV-positive adult patients who complete an initial encounter at a study cluster and at least one return encounter during the study period will be included ...
Source: Trials - April 9, 2015 Category: Research Source Type: clinical trials

Recruitment results among families contacted for an obesity prevention intervention: the Obesity Prevention Tailored for Health Study
Conclusions Recruiting parents and children into an obesity prevention program in a healthcare setting proved to be challenging and resource-intensive. Barriers and incentives for participation in obesity prevention programs need to be identified and addressed. Concern for the weight of their children may motivate parents to participate in family-based lifestyle interventions; however, the healthcare setting may be more relevant to weight-related treatment than to primary prevention. Trial registration Trial Registra...
Source: Trials - November 27, 2014 Category: Research Source Type: clinical trials