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Improving Parental Psychosocial Functioning and Early Developmental Outcomes in Children With Sickle Cell Disease

T

The University of The West Indies

Status

Completed

Conditions

Psychological Stress
Parenting
Cognitive Ability, General
Sickle Cell Disease

Treatments

Behavioral: Play therapy
Other: Problem solving skills

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

There are all significant risk factors for poor early cognitive development and, as such, neurocognitive deficits have been demonstrated in pre-school children with sickle cell disease (SCD). This project assesses the efficacy of using an evidence-based early stimulation program, combined with components to help parents cope with stress, delivered during six routine monthly clinic visits to parents of children with sickle cell disease. It is hoped that this innovation will improve parental psychological outcomes, as well as child developmental outcomes.

Full description

Children with sickle cell disease (SCD) are at risk of various complications, many of which arise suddenly and call on the problem solving skills of their parents. They are also at risk of neurocognitive delays; these may become evident during the pre-school years. Previous research by this group has demonstrated improved developmental outcomes after parental interventions incorporating play techniques in high risk and healthy pre-school children. The aim of the study is to determine usefulness in children with SCD of similar developmental interventions augmented by lessons in problem solving.

The study is a randomized controlled trial. Parents of all infants with Hb SS (homozygous sickle cell disease) or Sβ0 -thalassemia disease identified by newborn screening during the initial year of the study will be invited to participate. They will be randomized to intervention or control. Parental stress, infant's development and hemoglobin levels will be measured at recruitment and again after six months. The intervention will occur during monthly Penadur (intramuscular Benzathine Penicillin) visits and will include supervised play with their children using an inexpensive toy and participation in solving a problem which may arise as they parent their child with SCD. At the end of the study, all control dyads will also be given the toys used in the intervention. All parents will be given the results of their children's developmental assessments and appropriate referrals made if deficits are identified.

The study is minimal risk. Every effort will be made to maintain patient confidentiality. Respect for, and the maximum protection of the best interests of the research subjects will be maintained.

Enrollment

64 patients

Sex

All

Ages

6 to 12 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Infant has sickle cell disease: SS or Sβ0 thalassemia
  • Attending Sickle Cell Unit, Jamaica for routine care

Exclusion criteria

  • None

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

64 participants in 2 patient groups

Control
No Intervention group
Description:
The control dyad will receive usual care.
Intervened
Experimental group
Description:
Parents receive training in problem solving skills and play therapy with their infants.
Treatment:
Behavioral: Play therapy
Other: Problem solving skills

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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