[PDF] Top 20 Testing the 4Rs and 2Ss Multiple Family Group intervention: study protocol for a randomized controlled trial

... This study, a Hybrid Type II effectiveness-implementation research trial, blends clinical effectiveness and implementation research methods to examine the impact of the 4Rs and 2Ss ... See full document

... this group intervention program of eight sessions will be tested in a randomised controlled trial (RCT) with N = 182 adolescents aged 12 – 16, allocated to either the target ... See full document

... require multiple in-person visits to the clinic in the course of a few ...initial testing in schizophrenia [52, 65, 75], and are not used, to the best of our knowledge, in any clinical treat- ment ... See full document

... recent randomized trials are testing the effect of lifestyle interventions after pregnancy among women with GDM with the aim of preventing ...such trial randomized 450 women with GDM and im- ... See full document

... present intervention because it was proposed that both the nurse and the caregiver will combine their respective knowledge and experience to optimize the delirium management ...experimental intervention, ... See full document

... this study has several key strengths. It consists of a meditation intervention specif- ically based on MS features and needs, aimed at improv- ing the management of MS symptoms, such as numbness, fatigue, ... See full document

... The study is a two-arm RCT that analyzes the imple- mentation and effectiveness of a multi-component inter- vention on weight loss promotion tailored for South ...The intervention consists of two components ... See full document

... Patients are eligible if they are aged 45 years and older and have a diagnosis of possible or probable AD, includ- ing those patients who may have a mixed dementia. Ori- ginal eligibility criteria included age 65 years ... See full document

... Depression is associated with a range of problems, like school dropout, school difficulties, health problems, in- creased substance abuse, suicide, as well as problems with peers and family [18–21]. Furthermore, ... See full document

... present study will have some limitations that should be ...the study will only include families, who are willing to ...a family refuses to participate, the reason for refusal will be ...all ... See full document

... This trial faces a number of challenges which will need to be overcome if we are to recruit to ...being randomized to “treatment as usual,” which many consider ...this study (such as those judged at ... See full document

... facilitate group processes in CP and content fidelity are known to associate with signifi- cant reductions in preterm birth and intensive utilization of care ...the intervention period (CP-participants and ... See full document

... A study by Nordberg and colleagues [5] suggested that the amount of informal care that people with dementia receive is greater than the amount of formal care (6 h/day compared to 1 h/ day) even in the generous ... See full document

... to trial arm allocation being revealed to the women in order that knowledge of the type of care they will receive does not influence their ...the trial, will be given a hard copy (and an ad- dressed/postage ... See full document

... This study follows the principles of the Declaration of Helsinki (Version Edinburgh ...detailed study information, while partici- pants can ask questions by phone, e-mail, and face to ...This study ... See full document

... 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 ...the study period and ... See full document

... the trial will be in accordance with CONSORT guide- lines for cluster randomized trials [30, ...as randomized without imputation of miss- ing data, and with due emphasis placed on confidence ... See full document

... this study, reliable functional scales are used, such as the MFM, as well as timed tests that have clinically meaningful endpoints[47] and that are sufficiently sensi- tive to detect therapy related ...extremity ... See full document

... In addition to filling out an e-mail address, eligible subjects are asked to (voluntarily) fill out additional information on gender, age, educational level, social situation (living alone of together), current use of ... See full document

... A randomized controlled pilot trial with three measure- ment points will be carried out over 3 months to evalu- ate whether the intervention sustains an effect on the participants’ adherence ... See full document