Literature DB >> 25664228

The Cellie Coping Kit for Sickle Cell Disease: Initial acceptability and feasibility.

Meghan L Marsac1, Olivia G Klingbeil2, Aimee K Hildenbrand2, Melissa A Alderfer3, Nancy Kassam-Adams4, Kim Smith-Whitley5, Lamia P Barakat6.   

Abstract

Sickle Cell Disease (SCD) and its treatment can place physical and psychosocial strain on children and their families, underlining the need for behavioral and emotional support. Much of SCD is often managed at home, which may prevent children from obtaining supportive services from medical and psychosocial teams. Children with SCD report a restricted number of coping strategies specific to managing SCD and may benefit from education on adaptive coping. To address this unmet need, a coping tool for children with cancer (Cellie Cancer Coping Kit) was adapted for children with SCD. The Cellie Coping Kit for SCD (Cellie Coping Kit) includes a stuffed "Cellie" toy, coping cards for children, and a book for caregivers. This study sought to assess the acceptability and feasibility of an intervention utilizing the Cellie Coping Kit. Fifteen children with SCD (ages 6-14) and their caregivers participated in a baseline assessment including semi-structured interviews to examine SCD-related stressors and coping strategies. Next, families received a brief introduction to the Cellie Coping Kit and were provided with a kit to use independently over the next four weeks before completing a follow-up assessment. Results indicated strong intervention acceptability overall. While families reported using and learning information and skills from the Cellie Coping Kit, several challenges were identified (e.g., child's living situation, busy schedules). The Cellie Coping Kit is a promising tool to support children with SCD and their families. Future research should examine whether use of the Cellie Coping Kit impacts behavioral change and improved health outcomes.

Entities:  

Keywords:  coping; coping tool; family intervention; sickle cell disease

Year:  2014        PMID: 25664228      PMCID: PMC4315192          DOI: 10.1037/cpp0000062

Source DB:  PubMed          Journal:  Clin Pract Pediatr Psychol        ISSN: 2169-4826


  20 in total

Review 1.  A review of empirically supported psychosocial interventions for pain and adherence outcomes in sickle cell disease.

Authors:  Edith Chen; Steve W Cole; Pamela M Kato
Journal:  J Pediatr Psychol       Date:  2004 Apr-May

2.  Management of vaso-occlusive pain in children with sickle cell disease.

Authors:  Eufemia Jacob; Christine Miaskowski; Marilyn Savedra; Judith E Beyer; Marsha Treadwell; Lori Styles
Journal:  J Pediatr Hematol Oncol       Date:  2003-04       Impact factor: 1.289

3.  Coping with stressful events in older children and young adolescents.

Authors:  B E Compas; V L Malcarne; K M Fondacaro
Journal:  J Consult Clin Psychol       Date:  1988-06

4.  Posttraumatic stress disorder in children affected by sickle-cell disease and their parents.

Authors:  Michel Hofmann; Mariane de Montalembert; Bérengère Beauquier-Maccotta; Philippe de Villartay; Bernard Golse
Journal:  Am J Hematol       Date:  2007-02       Impact factor: 10.047

5.  Pain, quality of life, and coping in sickle cell disease.

Authors:  P Fuggle; P A Shand; L J Gill; S C Davies
Journal:  Arch Dis Child       Date:  1996-09       Impact factor: 3.791

Review 6.  Psychological therapies for sickle cell disease and pain.

Authors:  Kofi A Anie; John Green
Journal:  Cochrane Database Syst Rev       Date:  2012-02-15

7.  Quality of life of female caregivers of children with sickle cell disease: a survey.

Authors:  Xandra W van den Tweel; Janneke Hatzmann; Elske Ensink; Johanna H van der Lee; Marjolein Peters; Karin Fijnvandraat; Martha Grootenhuis
Journal:  Haematologica       Date:  2008-03-05       Impact factor: 9.941

8.  Sickle cell disease in children and adolescents: the relation of child and parent pain coping strategies to adjustment.

Authors:  K M Gil; D A Williams; R J Thompson; T R Kinney
Journal:  J Pediatr Psychol       Date:  1991-10

Review 9.  Sickle cell anaemia: progress in pathogenesis and treatment.

Authors:  Samir K Ballas
Journal:  Drugs       Date:  2002       Impact factor: 9.546

10.  Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress.

Authors:  Lamia P Barakat; Chavis A Patterson; Lauren C Daniel; Carlton Dampier
Journal:  Health Qual Life Outcomes       Date:  2008-08-09       Impact factor: 3.186

View more
  1 in total

1.  Improving self-management in adolescents with sickle cell disease.

Authors:  Lori E Crosby; Anna Hood; Katherine Kidwell; Cara Nwankwo; James Peugh; Heather Strong; Charles Quinn; Maria T Britto
Journal:  Pediatr Blood Cancer       Date:  2020-07-22       Impact factor: 3.167

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.