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Completed

NCT Number: NCT04056884

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

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.

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Key information

Age range

8 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Oslo

Oslo, Norge, 0317, Norway

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.
  • One parent able to attend the intervention.

Exclusion criteria

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

Treatment and study plan

SIBS intervention

Behavioral

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

Primary outcomes

  1. Strengths and difficulties questionnaire (SDQ)

    Time frame: Pre to 12-months follow-up

    Sibling mental health, reported by siblings, parents, and main teacher

Secondary outcomes

  1. Parent Child Communication Scale (PCCS)

    Time frame: Pre to 12-months follow-up

    Family communication, reported by siblings and parents

  2. KINDL Fragebogen (KINDL)

    Time frame: Pre to 12-months follow-up

    Sibling quality of life, rated by siblings and parents

  3. Sibling Knowledge Interview (SKI)

    Time frame: Pre to 12-months follow-up

    Sibling disorder knowledge based on brief interview

  4. Negative Adjustment Scale (NAS)

    Time frame: Pre to 12-months follow-up

    Sibling adaption, reported by siblings

Sponsors and collaborators

Lead sponsor

University of Oslo

Other

Collaborators

  • Lovisenberg Diakonale Hospital
  • Sykehuset Innlandet HF

Registry information

Official study title

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

Acronym: SIBS-RCT

Important dates

Study start
2019
Primary completion
2023
Study completion
2024
First posted
Aug 14, 2019
Registry last updated
Sep 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.