The CHIP-Family study to improve the psychosocial wellbeing of young children with congenital heart disease and their families: design of a randomized controlled trial

Malindi van der Mheen, Ingrid M van Beynum, Karolijn Dulfer, Jan van der Ende, Eugène van Galen, Jorieke Duvekot, Lisette E Rots, Tabitha P L van den Adel, Ad J J C Bogers, Christopher G McCusker, Frank A Casey, Willem A Helbing, Elisabeth M W J Utens, Malindi van der Mheen, Ingrid M van Beynum, Karolijn Dulfer, Jan van der Ende, Eugène van Galen, Jorieke Duvekot, Lisette E Rots, Tabitha P L van den Adel, Ad J J C Bogers, Christopher G McCusker, Frank A Casey, Willem A Helbing, Elisabeth M W J Utens

Abstract

Background: Children with congenital heart disease (CHD) are at increased risk for behavioral, emotional, and cognitive problems. They often have reduced exercise capacity and participate less in sports, which is associated with a lower quality of life. Starting school may present more challenges for children with CHD and their families than for families with healthy children. Moreover, parents of children with CHD are at risk for psychosocial problems. Therefore, a family-centered psychosocial intervention for children with CHD when starting school is needed. Until now, the 'Congenital Heart Disease Intervention Program (CHIP) - School' is the only evidence-based intervention in this field. However, CHIP-School targeted parents only and resulted in non-significant, though positive, effects as to child psychosocial wellbeing. Hence, we expanded CHIP by adding a specific child module and including siblings, creating the CHIP-Family intervention. The CHIP-Family study aims to (1) test the effects of CHIP-Family on parental mental health and psychosocial wellbeing of CHD-children and to (2) identify baseline psychosocial and medical predictors for the effectiveness of CHIP-Family.

Methods: We will conduct a single-blinded randomized controlled trial comparing the effects of CHIP-Family with care as usual (no psychosocial intervention). Children with CHD (4-7 years old) who are starting or attending kindergarten or primary school (first or second year) at the time of first assessment and their families are eligible. CHIP-Family consists of a separate one-day workshop for parents and children. The child workshop consists of psychological exercises based on the evidence-based cognitive behavioral therapy Fun FRIENDS protocol and sports exercises. The parent workshop focuses on problem prevention therapy, psychoeducation, general parenting skills, skills specific to parenting a child with CHD, and medical issues. Approximately 4 weeks after the workshop, parents receive an individual follow-up session. The baseline (T1) and follow-up assessment (T2 = 6 months after T1) consist of online questionnaires filled out by the child, parents, and teacher (T2 only). Primary outcome measures are the CBCL for children and the SCL-90-R for parents.

Discussion: This trial aims to test the effects of an early family-centered psychosocial intervention to meet the compelling need of young children with CHD and their families to prevent (further) problems. If CHIP-Family proves to be effective, it should be structurally implemented in standard care.

Trial registration: Dutch Trial Registry; NTR6063 on 23 August, 2016.

Keywords: CHIP; Children; Congenital heart defects; Families; Intervention; Psychosocial wellbeing.

Conflict of interest statement

Ethics approval and consent to participate

The Medical Ethics Committee of the Erasmus Medical Center approved this trial (NL56872.078.16). This study was registered in the Dutch Trial Registry (NTR6063). This study will be conducted according to the Helsinki Declaration. Informed written consents will be obtained from the parents or guardians of the participating children.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

    1. Marino BS, Lipkin PH, Newburger JW, Peacock G, Gerdes M, Gaynor JW, Mussatto KA, Uzark K, Goldberg CS, Johnson WH, Jr, et al. Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association. Circulation. 2012;126(9):1143–1172. doi: 10.1161/CIR.0b013e318265ee8a.
    1. McCusker CG, Doherty NN, Molloy B, Rooney N, Mulholland C, Sands A, Craig B, Stewart M, Casey F. A randomized controlled trial of interventions to promote adjustment in children with congenital heart disease entering school and their families. J Pediatr Psychol. 2012;37(10):1089–1103. doi: 10.1093/jpepsy/jss092.
    1. Van Rijen EH, Utens EM, Roos-Hesselink JW, Meijboom FJ, van Domburg RT, Roelandt JR, Bogers AJ, Verhulst FC. Psychosocial functioning of the adult with congenital heart disease: a 20-33 years follow-up. Eur Heart J. 2003;24(7):673–683. doi: 10.1016/S0195-668X(02)00749-2.
    1. Spijkerboer AW, Utens EM, Bogers AJ, Helbing WA, Verhulst FC. A historical comparison of long-term behavioral and emotional outcomes in children and adolescents after invasive treatment for congenital heart disease. J Pediatr Surg. 2008;43(3):534–539. doi: 10.1016/j.jpedsurg.2007.10.037.
    1. Utens EM, Verhulst FC, Meijboom FJ, Duivenvoorden HJ, Erdman RA, Bos E, Roelandt JT, Hess J. Behavioural and emotional problems in children and adolescents with congenital heart disease. Psychol Med. 1993;23(2):415–424. doi: 10.1017/S0033291700028518.
    1. Karsdorp PA, Everaerd W, Kindt M, Mulder BJ. Psychological and cognitive functioning in children and adolescents with congenital heart disease: a meta-analysis. J Pediatr Psychol. 2007;32(5):527–541. doi: 10.1093/jpepsy/jsl047.
    1. Menahem S, Poulakis Z, Prior M. Children subjected to cardiac surgery for congenital heart disease. Part 1 - emotional and psychological outcomes. Interact Cardiovasc Thorac Surg. 2008;7(4):600–604. doi: 10.1510/icvts.2007.171058.
    1. Bellinger DC, Newburger JW. Neuropsychological, psychosocial, and quality-of-life outcomes in children and adolescents with congenital heart disease. Prog Pediatr Cardiol. 2010;29(2):87–92. doi: 10.1016/j.ppedcard.2010.06.007.
    1. Wernovsky G. Current insights regarding neurological and developmental abnormalities in children and young adults with complex congenital cardiac disease. Cardiol Young. 2006;16(Suppl 1):92–104. doi: 10.1017/S1047951105002398.
    1. Opic P, Roos-Hesselink JW, Cuypers JA, Witsenburg M, van den Bosch A, van Domburg RT, Bogers AJ, Utens EM. Psychosocial functioning of adults with congenital heart disease: outcomes of a 30-43 year longitudinal follow-up. Clin Res Cardiol. 2015;104(5):388–400. doi: 10.1007/s00392-014-0792-1.
    1. Zomer AC, Vaartjes I, Uiterwaal CS, van der Velde ET, Sieswerda GJ, Wajon EM, Plomp K, van Bergen PF, Verheugt CL, Krivka E, et al. Social burden and lifestyle in adults with congenital heart disease. Am J Cardiol. 2012;109(11):1657–1663. doi: 10.1016/j.amjcard.2012.01.397.
    1. Dulfer K, Helbing WA, Duppen N, Utens EMWJ. Associations between exercise capacity, physical activity, and psychosocial functioning in children with congenital heart disease: a systematic review. Eur J Prev Cardiol. 2014;21(10):1200–1215. doi: 10.1177/2047487313494030.
    1. Dulfer K, Duppen N, Kuipers IM, Schokking M, van Domburg RT, Verhulst FC, Helbing WA, Utens EM. Aerobic exercise influences quality of life of children and youngsters with congenital heart disease: a randomized controlled trial. J Adolesc Health. 2014;55(1):65–72. doi: 10.1016/j.jadohealth.2013.12.010.
    1. McCusker CG, Doherty NN, Molloy B, Rooney N, Mulholland C, Sands A, Craig B, Stewart M, Casey F. A controlled trial of early interventions to promote maternal adjustment and development in infants born with severe congenital heart disease. Child Care Health Dev. 2010;36(1):110–117. doi: 10.1111/j.1365-2214.2009.01026.x.
    1. Jackson AC, Liang RPT, Frydenberg E, Higgins RO, Murphy BM. Parent education programmes for special health care needs children: a systematic review. J Clin Nurs. 2016;25(11–12):1528–1547. doi: 10.1111/jocn.13178.
    1. Landolt MA, Ystrom E, Stene-Larsen K, Holmstrom H, Vollrath ME. Exploring causal pathways of child behavior and maternal mental health in families with a child with congenital heart disease: a longitudinal study. Psychol Med. 2014;44(16):3421–3433. doi: 10.1017/S0033291713002894.
    1. Casey FA, Stewart M, McCusker CG, Morrison ML, Molloy B, Doherty N, Craig BG, Sands AJ, Rooney N, Mulholland HC. Examination of the physical and psychosocial determinants of health behaviour in 4-5-year-old children with congenital cardiac disease. Cardiol Young. 2010;20(5):532–537. doi: 10.1017/S1047951110000673.
    1. Lawoko S, Soares JJ. Quality of life among parents of children with congenital heart disease, parents of children with other diseases and parents of healthy children. Qual Life Res. 2003;12(6):655–666. doi: 10.1023/A:1025114331419.
    1. Lawoko S, Soares JJ. Psychosocial morbidity among parents of children with congenital heart disease: a prospective longitudinal study. Heart Lung. 2006;35(5):301–314. doi: 10.1016/j.hrtlng.2006.01.004.
    1. Tong EM, Kools S. Health care transitions for adolescents with congenital heart disease: patient and family perspectives. Nurs Clin North Am. 2004;39(4):727–740. doi: 10.1016/j.cnur.2004.07.011.
    1. Lesch W, Specht K, Lux A, Frey M, Utens E, Bauer U. Disease-specific knowledge and information preferences of young patients with congenital heart disease. Cardiol Young. 2014;24(2):1–10.
    1. Utens E, Callus E, Levert E, De Groote K, Casey F. Multidisciplinary family-centred psychosocial care for patients with CHD: consensus recommendations from the AEPC psychosocial working group. Cardiol Young. 2017;28(2):1–7.
    1. Levert EM, Helbing WA, Dulfer K, van Domburg RT, Utens EM. Psychosocial needs of children undergoing an invasive procedure for a CHD and their parents. Cardiol Young. 2016;27(2):1–12.
    1. Spijkerboer AW, Utens EMWJ, Bogers AJJC, Verhulst FC, Helbing WA. Long-term intellectual functioning and school-related behavioural outcomes in children and adolescents after invasive treatment for congenital heart disease. Br J Dev Psychol. 2008;26(4):457–470. doi: 10.1348/026151007X253323.
    1. Pahl KM, Barrett PM. Preventing anxiety and promoting social and emotional strength in preschool children: a universal evaluation of the fun FRIENDS program. Adv School Ment Health Promot. 2010;3(3):14–25. doi: 10.1080/1754730X.2010.9715683.
    1. Schulz KF, Altman DG, Moher D. CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. J Pharmacol Pharmacother. 2010;1(2):100–107. doi: 10.4103/0976-500X.72352.
    1. Achenbach TM, Rescorla LA. Manual for the ASEBA school-age forms & profiles. Burlington: University of Vermont, Research Center for Children, Youth, & Families; 2001.
    1. Achenbach TM, Becker A, Dopfner M, Heiervang E, Roessner V, Steinhausen HC, Rothenberger A. Multicultural assessment of child and adolescent psychopathology with ASEBA and SDQ instruments: research findings, applications, and future directions. J Child Psychol Psychiatry. 2008;49(3):251–275. doi: 10.1111/j.1469-7610.2007.01867.x.
    1. Arrindell WA, Ettema JHM. SCL-90. Symptom checklist. Handleiding bij een multidimensionele psychopathologie-indicator. Lisse: Swets Test Publishers; 2003.
    1. Utens EMWJ, Dulfer K. Rotterdams Kwaliteit van Leven Interview. 2010.
    1. Utens EMWJ, Dulfer K. Rotterdam knowledge questionnaire. 2010.
    1. Achenbach TM, Rescorla LA. Manual for ASEBA Preschool Forms & Profiles. Burlington: University of Vermont, Research Center for Children, Youth and Families; 2000.
    1. Verhulst FC, van der Ende J. Handleiding ASEBA Vragenlijsten voor leeftijden 6 tot en met 18 jaar. Rotterdam: ASEBA; 2013.
    1. Smidts DP, Huizinga M. BRIEF Executieve Functies Gedragsvragenlijst: Handleiding. Amsterdam: Hogrefe Uitgevers; 2009.
    1. Gioia GA, Isquith PK, Guy SC, Kenworthy L. Behavior rating inventory of executive function. Odessa: Psychological Assessment Resources Inc; 2000.
    1. Van der Heijden KB, Suurland J, De Sonneville LMJ, Swaab HJT. BRIEF-P Vragenlijst executieve functies voor 2- tot 5-jarigen. Amsterdam: Hogrefe uitgevers; 2013.
    1. Stevens M, Moget P, de Greef MH, Lemmink KA, Rispens P. The Groningen enjoyment questionnaire: a measure of enjoyment in leisure-time physical activity. Percept Mot Skills. 2000;90(2):601–604. doi: 10.2466/pms.2000.90.2.601.
    1. Dulfer K, Duppen N, Blom NA, van Dijk AP, Helbing WA, Verhulst FC, Utens EM. Effect of exercise training on sports enjoyment and leisure-time spending in adolescents with complex congenital heart disease: the moderating effect of health behavior and disease knowledge. Congenit Heart Dis. 2014;9(5):415–423. doi: 10.1111/chd.12154.
    1. Van der Heiden C, Muris P, Bos AE, van der Molen HT. Factor structure of the Dutch version of the Penn State worry questionnaire. J Behav Ther Exp Psychiatry. 2010;41(3):304–309. doi: 10.1016/j.jbtep.2010.02.009.
    1. Brock AJLL, Vermulst AA, Gerris JRM, Abidin RR. NOSI, Nijmeegse Ouderlijke Stress Index, handleiding. 1992.
    1. Abidin RR. Parenting stress index. 3. Lutz: Psychological Assessments Resources, Inc; 1983.
    1. Haverman L, van Oers HA, Limperg PF, Houtzager BA, Huisman J, Darlington AS, Maurice-Stam H, Grootenhuis MA. Development and validation of the distress thermometer for parents of a chronically ill child. J Pediatr. 2013;163(4):1140–1146. doi: 10.1016/j.jpeds.2013.06.011.
    1. Langraf JM, Abetz L, Ware JE. The CHQ user’s manual. Boston: Health Act; 1999.
    1. Garnefski N, Rieffe C, Jellesma F, Terwogt MM, Kraaij V. Cognitive emotion regulation strategies and emotional problems in 9 - 11-year-old children: the development of an instrument. Eur Child Adolesc Psychiatry. 2007;16(1):1–9. doi: 10.1007/s00787-006-0562-3.
    1. Epstein NB, Baldwin LM, Bishop DS. The McMaster family assessment device. J Marital Fam Ther. 1983;9(2):171–180. doi: 10.1111/j.1752-0606.1983.tb01497.x.
    1. Hofstra MB, van der Ende J, Verhulst FC. Child and adolescent problems predict DSM-IV disorders in adulthood: a 14-year follow-up of a Dutch epidemiological sample. J Am Acad Child Adolesc Psychiatry. 2002;41(2):182–189. doi: 10.1097/00004583-200202000-00012.
    1. Law EF, Fisher E, Fales J, Noel M, Eccleston C. Systematic review and meta-analysis of parent and family-based interventions for children and adolescents with chronic medical conditions. J Pediatr Psychol. 2014;39(8):866–886. doi: 10.1093/jpepsy/jsu032.
    1. D’Zurilla TJ, Nezu AM. Problem-solving therapy. In: Dobson KS, editor. Handbook of cognitive-behavioral therapies. 3. New York: The Guilford Press; 2010.
    1. Meyer TJ, Miller ML, Metzger RL, Borkovec TD. Development and validation of the Penn State worry questionnaire. Behav Res Ther. 1990;28(6):487–495. doi: 10.1016/0005-7967(90)90135-6.
    1. Tuinman MA, Gazendam-Donofrio SM, Hoekstra-Weebers JE. Screening and referral for psychosocial distress in oncologic practice: use of the distress thermometer. Cancer. 2008;113(4):870–878. doi: 10.1002/cncr.23622.
    1. Hullmann SE, Ryan JL, Ramsey RR, Chaney JM, Mullins LL. Measures of general pediatric quality of life: child health questionnaire (CHQ), DISABKIDS chronic generic measure (DCGM), KINDL-R, pediatric quality of life inventory (PedsQL) 4.0 generic Core scales, and quality of my life questionnaire (QoML) Arthritis Care Res. 2011;63(Suppl 11):S420–S430. doi: 10.1002/acr.20637.
    1. Aaronson NK, Muller M, Cohen PD, Essink-Bot ML, Fekkes M, Sanderman R, Sprangers MA, te Velde A, Verrips E. Translation, validation, and norming of the Dutch language version of the SF-36 health survey in community and chronic disease populations. J Clin Epidemiol. 1998;51(11):1055–1068. doi: 10.1016/S0895-4356(98)00097-3.
    1. Epstein L. Family and community medicine: complementary components of primary health care. Isr J Med Sci. 1983;19(8):719–722.

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