Skip to content

SIBS-Intervention for Siblings and Parents of Children With Chronic Illness

A Randomized Controlled Group Intervention Trial for Siblings and Parents of Children With Chronic Illness (SIBS-RCT)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04056884
Acronym
SIBS-RCT
Enrollment
288
Registered
2019-08-14
Start date
2019-09-01
Completion date
2024-09-30
Last updated
2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Siblings of Children With Chronic Illness

Brief summary

SIBS-RCT is a randomized controlled trial comparing the effect of a 5-session group intervention for siblings and parents of children with chronic illness to 12-week waitlist. Participants randomized to waitlist will receive the intervention after waitlist. The main outcome is sibling mental health, and secondary outcomes include family communication, sibling disorder knowledge, quality of life, and adaption. Outcomes will be examined at pre-, post, 3-, 6- and 12- month follow-up.

Detailed description

Siblings' wellbeing is at risk when one's brother or sister has a neurodevelopmental disorder. Neurodevelopmental disorders are enduring somatic and/or mental conditions affecting the central nervous system, such as autism, intellectual disability, and cerebral palsy. The mechanisms behind the wellbeing risk for siblings are linked to siblings' lack of disorder knowledge, poor parental mental health due to extra care responsibilities, and impaired family communication. No evidence-based interventions to improve sibling wellbeing exist. To address this gap, we propose examining a group intervention for siblings and parents of children with neurodevelopmental disorders in a randomized controlled trial (SIBS-RCT). SIBS-RCT compares a 5-session manual-based sibling-parent group intervention delivered over two weeks, to 3-month treatment as usual waitlist. The planned sample is 288 siblings and 288 parents. Recruitment and intervention will take place in specialist and municipal health services. Inclusion criteria are being the sibling (aged 8-16 years) of a child (aged 0-18 years) who is diagnosed with neurodevelopmental disorder and who receives specialist or municipal health services. Participants will be randomized in blocks of 6 to intervention or waitlist. The primary outcome is sibling mental health. Secondary outcomes include quality of life, disorder knowledge, and family communication. Predictor measures include biological stress levels, parent mental health, disorder impairment, and group leader adherence to the SIBS-manual. Measures will be electronically rated by siblings, parents, and teachers at pre-intervention, post-intervention, and 3, 6, and 12 months follow-up. Main effects of the intervention will be measured as the mean mental health change difference between intervention and waitlist from pre-intervention to 3-month follow-up. We will also apply growth curve models to examine trajectories of outcomes from pre-intervention to 12-month follow-up. Expected outcomes include improved sibling wellbeing, improved health services for siblings and families of children with neurodevelopmental disorders, and better integration between municipal and specialist services.

Interventions

BEHAVIORALSIBS intervention

SIBS is a manual-based group intervention for siblings and parents of children with chronic illness

Sponsors

Sykehuset Innlandet HF
CollaboratorOTHER
Lovisenberg Diakonale Hospital
CollaboratorOTHER
University of Oslo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Masking description

N/A, not possible

Intervention model description

Participants are randomized to intervention or 12-week waitlist. All participants who are randomized to waitlist will receive the intervention after waitlist.

Eligibility

Sex/Gender
ALL
Age
8 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

1. Being the sibling of a child diagnosed with chronic illness who is aged 0 to 18 years and receives specialist and/or municipal health services. 2. One parent able to attend the intervention.

Exclusion criteria

1. Being enrolled as primary patients in specialist health services; 2. Chronic illness diagnosis.

Design outcomes

Primary

MeasureTime frameDescription
Strengths and difficulties questionnaire (SDQ)Pre to 12-months follow-upSibling mental health, reported by siblings, parents, and main teacher

Secondary

MeasureTime frameDescription
Parent Child Communication Scale (PCCS)Pre to 12-months follow-upFamily communication, reported by siblings and parents
KINDL Fragebogen (KINDL)Pre to 12-months follow-upSibling quality of life, rated by siblings and parents
Sibling Knowledge Interview (SKI)Pre to 12-months follow-upSibling disorder knowledge based on brief interview
Negative Adjustment Scale (NAS)Pre to 12-months follow-upSibling adaption, reported by siblings

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026