[PDF] Top 20 FIT for FUNCTION: study protocol for a randomized controlled trial

... this trial are very broad so there will be a heterogeneous sample of participants with a wide range of function, fitness, and ages who will po- tentially ...the trial need to gain medical clearance ... See full document

... proprioceptive function of the affected joint compared with age-matched con- trols ...proprioceptive function and quadriceps strength is important for KOA ...lar function of healthy individuals, ... See full document

... All patients will be recruited via the ‘Midhagen’ out- patient unit for young adults (aged 18 to 45 years) with first-episode psychosis. Located in central Stockholm, the clinic delivers need-based care with the aim of ... See full document

... three randomized trials is already available with children as well [5, 30, 31], reviewed in ...meditation-relaxation protocol in reducing PTSD symptoms and functional im- pairment in 8–14-year-old Sri ... See full document

... present study aims to test the relative efficacy of two components added to TF- CBT focussing on parent-related aspects of IPV, namely parenting and parent-child interactions, and thereby pro- vides crucial ... See full document

... Artificial sweeteners, frequently used in Brazil to sweeten coffee and tea, have been recently shown to drive the development of glucose intolerance in rodents through direct compositional and functional alterations in ... See full document

... TRANSVERSAL trial is designed as a randomized controlled trial to compare transvaginal hybrid NOTES and laparoscopic-assisted sigmoid ... See full document

... TTT protocol, and made it possible to optimize the procedures and measures in the research ...the study enough power to investigate the effects of the TTT program and the wide range of functionally relevant ... See full document

... each study site are considered for the trial at the time of their visit to the outpatient depart- ment prior to ...the study is limited to no less than 20 ... See full document

... Preloop trial (Clinical Trials NCT03445936) is a prospective, randomized, controlled, multicenter trial to compare synthetic mesh (Parietene Macro ™ , Medtronic, Minneapolis, MN, USA) and ... See full document

... treatment effect (mean difference in KOOS scores) we will employ a random or fixed effects linear regression model with point estimates [62] and both crude and ad- justed results will be reported. The regression model ... See full document

... The study has been approved by the Institutional Review Broad of the University of Hong Kong/Hospital Authority Hong Kong West Cluster and has been registered under Clinical Trials Registry (trial number ... See full document

... this study provides 800 mg DHA in two (2) 1-g capsules and the higher DHA group of sub- jects will be asked to consume two capsules per ...previous trial, on average 74% of capsules were ... See full document

... Patients allocated to the dydrogesterone group will receive dydrogesterone 40 mg per os, followed by 10 mg per os three times a day, and an identical-looking pla- cebo will be used in the control group accordingly. Con- ... See full document

... This protocol paper outlines the background and design of a randomized controlled trial of Baby Triple P for first-time pregnant parents in high-risk ...this study will be the re- ... See full document

... The protocol described in this paper is of a pragmatic randomized controlled trial comparing eight sessions of telephone CBT to an active social control, referred to as ...this study ... See full document

... each study site. Study site is the stratification vari- able for this randomization ...each study site, a 1:1 allocation ...Each study site has a predefined set of patients to ...each ... See full document

... All data will be collected in personal CRFs, which will be stored in the patient’s own hospital. Copies of the completed forms will be sent to our coordinating center (Canisius-Wilhelmina Hospital, Nijmegen). All data ... See full document

... The rates for the primary endpoint: major morbidity, re- intervention and mortality for PC were 6.2, 13.1 and 12.7% respectively in the review and 22.2, 18.5 and 14.8% in our own series. We believe that the 6.2% ... See full document

... Bi-TPAI trial is a multicenter, parallel group, randomized, controlled, non-inferiority trial in patients with early ...Bi-TPAI trial will include 220 patients with HTG-AP from 17 large ... See full document