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Parents clinical trials

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NCT ID: NCT02278809 Completed - Physical Activity Clinical Trials

Promoting Healthy Lifestyle Behaviors in Schoolchildren: an Online Video Intervention for Parents

Movie Models
Start date: December 2013
Phase: N/A
Study type: Interventional

1. Development of a method for parents of primary schoolchildren to teach parents parenting skills to obtain health gain in the family through videos and online feedback. 2. Effect- and procesevaluation of this methodology. 3. Development of an implementation guide together with VIGEZ as primary partner and in association with partner organisations on the field.

NCT ID: NCT02234661 Completed - Children Clinical Trials

Expanding the Cycle of Opportunity: Simultaneously Educating Parents and Children in Head Start

CAPFAST
Start date: June 2014
Phase: N/A
Study type: Interventional

The CAP Family Advancement Study (CAP FAST) is a randomized control trial of CareerAdvance®, a dual-generation program providing education, career coaching, and soft-skills training for parents while their children attend CAP Tulsa's Head Start programs.

NCT ID: NCT01770093 Not yet recruiting - Parents Clinical Trials

Preferences of Parents for Pediatric Inpatient Ward Physicians' Attire

Start date: February 2013
Phase: N/A
Study type: Observational

Several studies have been conducted throughout the world to evaluate patients' and parents' preferences regarding physicians' attire. Most studies have shown that the attire influences their feelings trust and confidence regarding their care. In most countries the preference is for formal attire. In other places a more casual attire is generally accepted. Israel is a country where casual dress is acceptable in most settings. Israeli physician's dress code has been discussed in the past, but has never been systematically studied. The aim of this study is to systematically examine the attitudes of parents of children who have been admitted to the pediatric ward towards physicians' attire.

NCT ID: NCT01666548 Completed - Children Clinical Trials

Haemolytic Uraemic Syndrome in Childhood: Clinical, Cognitive and Psychological Aspects

Start date: February 2012
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the clinical, cognitive outcome and psychosocial outcome of haemolytic uraemic syndrome in childhood. The haemolytic uraemic syndrome (HUS) is the leading cause of acute renal failure in childhood. The more common typical HUS is mostly caused by Shigatoxin-producing enterohaemorrhagic Escherichia coli (EHEC). The rarer atypical HUS is mainly caused by different genetic abnormalities in complement regulatory proteins. About 50 till 60 percent of all patients with HUS develop a severe acute renal failure and require dialysis. Resulting from new diagnostic and therapeutic approaches the survival rate increased during the last years. Despite this, there are only few data concerning long-term prognosis, cognitive and motoric development, as well as psychological coping and health-related quality of life of affected children and their parents.

NCT ID: NCT00639470 Completed - Parents Clinical Trials

Parents Reading Comprehension of Their Child's Post-Operative Medicine Fact Sheets

Start date: August 2005
Phase: N/A
Study type: Interventional

The objective of this study is to test legal guardians reading comprehension of their child's post-operative medication administration using three different versions of written medication information (standard fact sheets, easy-to-read fact sheets, and easy-to-read fact sheets accompanied by illustrations).

NCT ID: NCT00543257 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Parents at the Center: Information Management in ADHD - Clinical Trial

Start date: December 2007
Phase: N/A
Study type: Observational

Health literacy is an integral part of the pathway for the successful transfer of information between patients and providers. Parents of children with Attention Deficit/ Hyperactivity Disorder (ADHD) play an essential role in chronic care as they offer critical information to providers that drives appropriate education and disease management. We propose the development and evaluation of an electronic data entry tool that enables parents to communicate data essential to treatment of their children, regardless of their own literacy skills. The research plan addresses a question central to patient-centered information management: how does health literacy influence parents' report of data on ADHD and the process-level events that result from parent-provider communication? The following specific aims organize the clinical study: proposal: 1) To assess the effect of health literacy on successful completion of parent-reported ADHD health information in both paper-based and PCHR formats, and, 2): To determine the association between health literacy and process-level outcomes for ADHD that stem from parent-provider exchange of information. The formal evaluation will study a diverse cohort of parents in a randomized trial of data entry (paper versus PCHR) for ADHD-specific information. Primary care records for children of this cohort will be analyzed for the prior 12 month period. Both a retrospective examination of documented ADHD processes of care and a prospective evaluation of the utility of data from the PCHR will occur. Literacy level is a primary variable of interest throughout the evaluation.