Literature DB >> 23995469

Reproductive health choices for young adults with sickle cell disease or trait: randomized controlled trial immediate posttest effects.

Diana J Wilkie1, Agatha M Gallo, Yingwei Yao, Robert E Molokie, Christine Stahl, Patricia E Hershberger, Zhongsheng Zhao, Marie L Suarez, Robert J Labotka, Bonnye Johnson, Rigo Angulo, Veronica Angulo, Jesus Carrasco, David Shuey, Stephanie Pelligra, Edward Wang, Dennie T Rogers, Alexis A Thompson.   

Abstract

BACKGROUND: People with sickle cell disease (SCD) or sickle cell trait (SCT) may not have information about genetic inheritance needed for making informed reproductive health decisions. CHOICES is a Web-based, multimedia educational intervention that provides information about reproductive options and consequences to help those with SCD or SCT identify and implement an informed parenting plan. Efficacy of CHOICES compared with usual care must be evaluated.
OBJECTIVE: The purpose was to compare immediate posttest effects of CHOICES versus an attention-control usual care intervention (e-Book) on SCD-/SCT-related reproductive health knowledge, intention, and behavior.
METHODS: In a randomized controlled study, we recruited subjects with SCD/SCT from clinics, community settings, and online networks with data collected at sites convenient to the 234 subjects with SCD (n = 136) or SCT (n = 98). Their ages ranged from 18 to 35 years; 65% were women, and 94% were African American. Subjects completed a measure of sickle cell reproductive knowledge, intention, and behavior before and immediately after the intervention.
RESULTS: Compared with the e-Book group, the CHOICES group had significantly higher average knowledge scores and probability of reporting a parenting plan to avoid SCD or SCD and SCT when pretest scores were controlled. Effects on intention and planned behavior were not significant. The CHOICES group showed significant change in their intention and planned behavior, whereas the e-Book group did not show significant change in their intention, but their planned behavior differed significantly. DISCUSSION: Initial efficacy findings are encouraging but warrant planned booster sessions and outcome follow-ups to determine sustained intervention efficacy on reproductive health knowledge, intention, and actual behavior of persons with SCD/SCT.

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Year:  2013        PMID: 23995469      PMCID: PMC3805179          DOI: 10.1097/NNR.0b013e3182a0316b

Source DB:  PubMed          Journal:  Nurs Res        ISSN: 0029-6562            Impact factor:   2.381


  33 in total

1.  A randomized, controlled pilot trial of a school intervention for children with sickle cell anemia.

Authors:  Kristine Koontz; Amy D Short; Karen Kalinyak; Robert B Noll
Journal:  J Pediatr Psychol       Date:  2004 Jan-Feb

2.  Prenatal genetic testing: an investigation of determining factors affecting the decision-making process.

Authors:  Monica Pivetti; Giannino Melotti
Journal:  J Genet Couns       Date:  2012-04-03       Impact factor: 2.537

3.  Adolescent pregnancy intentions and pregnancy outcomes: a longitudinal examination.

Authors:  Cynthia Rosengard; Maureen G Phipps; Nancy E Adler; Jonathan M Ellen
Journal:  J Adolesc Health       Date:  2004-12       Impact factor: 5.012

4.  Comparing three theories in predicting reproductive health behavioral intention in adolescent women with diabetes.

Authors:  Shiaw-Ling Wang; Denise Charron-Prochownik; Susan M Sereika; Linda Siminerio; Yookyung Kim
Journal:  Pediatr Diabetes       Date:  2006-04       Impact factor: 4.866

5.  Disease management, coping, and functional disability in pediatric sickle cell disease.

Authors:  Gloria Oliver-Carpenter; Ilana Barach; Lori E Crosby; Jessica Valenzuela; Monica J Mitchell
Journal:  J Natl Med Assoc       Date:  2011-02       Impact factor: 1.798

6.  A pilot study to explore knowledge, attitudes, and beliefs about sickle cell trait and disease.

Authors:  Kruti Acharya; Colleen Walsh Lang; Lainie Friedman Ross
Journal:  J Natl Med Assoc       Date:  2009-11       Impact factor: 1.798

7.  Attitudes and beliefs of African-Americans toward genetics, genetic testing, and sickle cell disease education and awareness.

Authors:  Katie A Long; Stephen B Thomas; Robin E Grubs; Elizabeth A Gettig; Lakshmanan Krishnamurti
Journal:  J Genet Couns       Date:  2011-07-12       Impact factor: 2.537

8.  The burden of emergency department use for sickle-cell disease: an analysis of the national emergency department sample database.

Authors:  Sophie Lanzkron; C Patrick Carroll; Carlton Haywood
Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

Review 9.  Health-related quality of life in sickle cell disease: past, present, and future.

Authors:  Julie A Panepinto; Melanie Bonner
Journal:  Pediatr Blood Cancer       Date:  2012-04-22       Impact factor: 3.167

10.  Sickle cell disease: the need for a public health agenda.

Authors:  Hussain R Yusuf; Michele A Lloyd-Puryear; Althea M Grant; Christopher S Parker; Melissa S Creary; Hani K Atrash
Journal:  Am J Prev Med       Date:  2011-12       Impact factor: 5.043

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  21 in total

1.  Reproductive Health CHOICES for Young Adults with Sickle Cell Disease or Trait: Randomized Controlled Trial Outcomes over Two Years.

Authors:  Agatha M Gallo; Diana J Wilkie; Yingwei Yao; Robert E Molokie; Christiane Stahl; Patricia E Hershberger; Zhongsheng Zhao; Marie L Suarez; Bonnye Johnson; Rigoberto Angulo; Jesus Carrasco; Veronica Angulo; Alexis A Thompson
Journal:  J Genet Couns       Date:  2015-08-28       Impact factor: 2.537

2.  Identifying Factors Underlying the Decision for Sickle Cell Carrier Screening Among African Americans Within Middle Reproductive Age.

Authors:  Tilicia L Mayo-Gamble; Susan E Middlestadt; Hsien-Chang Lin; Jennifer Cunningham-Erves; Priscilla Barnes; Pamela Braboy Jackson
Journal:  J Genet Couns       Date:  2018-03-24       Impact factor: 2.537

3.  Acceptability of Clinical Decision Support Interface Prototypes for a Nursing Electronic Health Record to Facilitate Supportive Care Outcomes.

Authors:  Janet Stifter; Vanessa E C Sousa; Alessandro Febretti; Karen Dunn Lopez; Andrew Johnson; Yingwei Yao; Gail M Keenan; Diana J Wilkie
Journal:  Int J Nurs Knowl       Date:  2017-09-19       Impact factor: 1.222

4.  Perception of young adults with sickle cell disease or sickle cell trait about participation in the CHOICES randomized controlled trial.

Authors:  Patricia E Hershberger; Agatha M Gallo; Robert Molokie; Alexis A Thompson; Marie L Suarez; Yingwei Yao; Diana J Wilkie
Journal:  J Adv Nurs       Date:  2015-06-15       Impact factor: 3.187

5.  Randomized clinical trial of computerized PAINRelieveIt® for patients with sickle cell disease: PAINReportIt® and PAINUCope®.

Authors:  Brenda W Dyal; Miriam O Ezenwa; Yingwei Yao; Robert E Molokie; Zaijie J Wang; Samir K Ballas; Marie L Suarez; Diana J Wilkie
Journal:  Patient Educ Couns       Date:  2019-08-17

6.  Sickle Cell Education: A Survey of Antenatal Healthcare Givers.

Authors:  Serwah Aboagye; Magdalene Torto; Kwaku Asah-Opoku; Mercy Anna Nuamah; Samuel Antwi Oppong; Ali Samba
Journal:  Am J Trop Med Hyg       Date:  2019-09       Impact factor: 2.345

7.  Toward understanding family-related characteristics of young adults with sickle-cell disease or sickle-cell trait in the USA.

Authors:  Patricia E Hershberger; Agatha M Gallo; Robert Molokie; Alexis A Thompson; Marie L Suarez; Yingwei Yao; Constance M Dallas; Diana J Wilkie
Journal:  J Clin Nurs       Date:  2016-03-11       Impact factor: 3.036

8.  Youth with Sickle Cell Disease: Genetic and Sexual Health Education Needs.

Authors:  Ashley J Housten; Regina A Abel; Joyce Dadekian; Kelly Schwieterman; Dawn Jason; Allison A King
Journal:  Am J Health Behav       Date:  2015-11

9.  Reproductive Life Planning: A Cross-Sectional Study of What College Students Know and Believe.

Authors:  Lisa N Kransdorf; T S Raghu; Juliana M Kling; Paru S David; Suneela Vegunta; Jo Knatz; Allan Markus; Keith A Frey; Yu-Hui H Chang; Anita P Mayer; Julia A Files
Journal:  Matern Child Health J       Date:  2016-06

Review 10.  Interventions for patients and caregivers to improve knowledge of sickle cell disease and recognition of its related complications.

Authors:  Monika R Asnani; Kim R Quimby; Nadia R Bennett; Damian K Francis
Journal:  Cochrane Database Syst Rev       Date:  2016-10-06
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