Literature DB >> 27822877

Feasibility and Preliminary Efficacy of an Internet Support Group for Parents of a Child with Neurofibromatosis Type 1: a Pilot Study.

S Martin1,2, M C Roderick3,4, R Lockridge3,4, M A Toledo-Tamula5, A Baldwin4, P Knight6, P Wolters3.   

Abstract

This pilot study investigated the feasibility and preliminary efficacy of an Internet Support Group (ISG) for parents of children with NF1. Eligible parents were recruited by email and completed baseline questionnaires assessing social support, self-efficacy, depression, and anxiety. The ISG involved eight weekly 90-min chat sessions and a discussion forum open 24 h/day for 8 weeks. Follow-up measures were completed immediately post-intervention and 3 months later. Parents from 33 families (29 mothers, 4 fathers) completed baseline measures. Over half of parents (52 %) rated their child's disease severity as mild, 33 % moderate, and 15 % severe. Among 21 parents who completed post-intervention measures, ratings of perceived emotional (p = .0008) and informational (p = .0003) support increased. There were no significant changes in self-efficacy, depression, or anxiety (ps > .05). The mean satisfaction rating was moderately high (7.6/10; range 4-10). Some parents commented that the chat sessions were at inconvenient times, which may have limited participation. Preliminary evidence in this small sample of parents suggests that ISGs may be a feasible and potentially efficacious method of providing support to parents of children with NF1. Having multiple weekly chat sessions held at various days and times may improve accessibility and participation. Clinicians are encouraged to help parents access online support resources.

Entities:  

Keywords:  Children; Internet support group; Neurofibromatosis type 1; Parents; Social support

Mesh:

Year:  2016        PMID: 27822877     DOI: 10.1007/s10897-016-0031-1

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  45 in total

1.  Risk factors for psychological maladjustment of parents of children with cancer.

Authors:  J E Hoekstra-Weebers; J P Jaspers; W A Kamps; E C Klip
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1999-12       Impact factor: 8.829

Review 2.  Clinical manifestations and management of neurofibromatosis type 1.

Authors:  James H Tonsgard
Journal:  Semin Pediatr Neurol       Date:  2006-03       Impact factor: 1.636

Review 3.  Adjustment and coping by parents of children with cancer: a review of the literature.

Authors:  M A Grootenhuis; B F Last
Journal:  Support Care Cancer       Date:  1997-11       Impact factor: 3.603

4.  Logging on: evaluating an online support group for parents of children with autism spectrum disorders.

Authors:  Tessen Clifford; Patricia Minnes
Journal:  J Autism Dev Disord       Date:  2013-07

5.  Gender response to neurofibromatosis 1.

Authors:  J Ablon
Journal:  Soc Sci Med       Date:  1996-01       Impact factor: 4.634

6.  Parents' experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study.

Authors:  Jenny Barke; Jane Coad; Diana Harcourt
Journal:  J Community Genet       Date:  2015-07-23

7.  Effect of Internet peer-support groups on psychosocial adjustment to cancer: a randomised study.

Authors:  M T Høybye; S O Dalton; I Deltour; P E Bidstrup; K Frederiksen; C Johansen
Journal:  Br J Cancer       Date:  2010-04-27       Impact factor: 7.640

8.  Impact of neurofibromatosis 1 upon quality of life in childhood: a cross-sectional study of 79 cases.

Authors:  P Wolkenstein; D Rodriguez; S Ferkal; H Gravier; V Buret; N Algans; M-C Simeoni; S Bastuji-Garin
Journal:  Br J Dermatol       Date:  2008-12-05       Impact factor: 9.302

9.  An interactive health communication application for supporting parents managing childhood long-term conditions: outcomes of a randomized controlled feasibility trial.

Authors:  Veronica M Swallow; Kathleen Knafl; Sheila Santacroce; Malcolm Campbell; Andrew G Hall; Trish Smith; Ian Carolan
Journal:  JMIR Res Protoc       Date:  2014-12-03

10.  Quality of life among parents of children with heart disease.

Authors:  Mostafa A Arafa; Salah R Zaher; Amira A El-Dowaty; Dalia E Moneeb
Journal:  Health Qual Life Outcomes       Date:  2008-11-03       Impact factor: 3.186

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  4 in total

1.  Supporting caregivers during hematopoietic cell transplantation for children with primary immunodeficiency disorders.

Authors:  Jennie Yoo; Meghan C Halley; E Anne Lown; Veronica Yank; Katherine Ort; Morton J Cowan; Morna J Dorsey; Heather Smith; Sumathi Iyengar; Christopher Scalchunes; Christina Mangurian
Journal:  J Allergy Clin Immunol       Date:  2018-10-25       Impact factor: 10.793

2.  An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis.

Authors:  Staci Martin; Kari L Struemph; Alyssa Poblete; Mary Anne Toledo-Tamula; Robin Lockridge; Marie Claire Roderick; Pamela Wolters
Journal:  J Community Genet       Date:  2018-03-02

3.  Exploring the Use of a Facebook-Based Support Group for Caregivers of Children and Youth With Complex Care Needs: Qualitative Descriptive Study.

Authors:  Katherine Jennifer Kelly; Shelley Doucet; Alison Luke; Rima Azar; William Montelpare
Journal:  JMIR Pediatr Parent       Date:  2022-06-07

4.  Experiences, Motivations, and Perceived Impact of Participation in a Facebook-Based Support Group for Caregivers of Children and Youth With Complex Care Needs: Qualitative Descriptive Study.

Authors:  Katherine Jennifer Kelly; Shelley Doucet; Alison Luke; Rima Azar; William Montelpare
Journal:  JMIR Pediatr Parent       Date:  2022-07-06
  4 in total

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