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Promotion of Positive Sibling RelationshipsSIBSNCT03706014

Innovative Family Prevention With Latino Siblings in Disadvantaged Settings

A study testing SIBS Program in people with Promotion of Positive Sibling Relationships, run by Harvard University at 1 site in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The current study is a randomized intervention trial that tests the efficacy of a family-focused sibling relationship promotion program. The study includes a treatment group and a contact-equivalent attention control condition with 288 sibling dyads and data collection with target parents, target sibling dyads, and… Read more about this study

Who is it for?
Ages 5 years and olderHealthy volunteers can take part
What is being tested?
SIBS Program
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
270 participants
Where
1 siteUnited States
Study dates
29 Sep 2018to 15 Dec 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 5 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Target child has to be a 5th grader
  • Target child has to be of Latino/Hispanic heritage
  • Target child has to have a younger sibling enrolled in the same school in the 1st through 4th grade
  • Target child and younger sibling have to be enrolled students in a participating elementary school.

Who cannot join

  • Enrollment in a self-contained special education setting

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Arizona State University

    Tempe, Arizona, 85287

Other trials in United States

About this study

The current study is a randomized intervention trial that tests the efficacy of a family-focused sibling relationship promotion program. The study includes a treatment group and a contact-equivalent attention control condition with 288 sibling dyads and data collection with target parents, target sibling dyads, and teachers at three time points (pre-test, post-test, and 18-month follow-up). Data will be collected using a three-cohort design with 96 families in each of the three cohorts.

Read the detailed description

The proposed project tests the efficacy of a family-focused program. This innovative program is focused on sibling relationships and parenting of siblings as synergistic targets of change to promote positive interpersonal family dynamics and parent and youth psychosocial and behavioral health and well-being. This translational effort builds on strong theoretical and empirical premises including a successful pilot study (ASU SIBS Program). Using a rigorous design and measurement, aims are to: (a) test the efficacy of SIBS, delivered via 12 weekly afterschool sibling sessions and 3 family nights in the familiar elementary school setting, versus a contact-equivalent attention control condition. Mexican-origin sibling dyads (5th graders and younger siblings; N = 288 dyads) and their parents will be recruited from economically disadvantaged elementary schools and randomly assigned within school to intervention or contact-equivalent attention control conditions. Assessments will be conducted at pre-test, post-test, and 18-month follow-up. Program effects will be tested on primary and secondary outcomes, including sibling relationship quality (i.e., warmth and negativity), sibling relationship skills, children's efficacy (social, emotional), children's internalizing symptoms, parents' stress and depressive symptoms, parent-child warmth and conflict, and family cohesion. Findings will advance prevention science by identifying an efficacious program that capitalizes on cultural assets to promote positive family dynamics and psychosocial well-being among Latinos, including by incorporating daily measurements of intervention targets (sibling relationship skills) to identify mechanisms underlying program effects.

Being tested
SIBS Program, Control
Keywords
siblings, family, Latinos, social emotional competencies, parenting, middle childhood, late childhood

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • SIBS ProgramBehavioural

    Universal prevention program promoting positive sibling and family relationships conducted in an afterschool setting

  • ControlBehavioural

    Contact-equivalent attention control program in which students play educational games

Study groups in NCT03706014
Study groupRoleWhat they receive
SIBS ProgramExperimentalThe program condition includes 12 weekly 90-minute afterschool group sessions for siblings. Sessions are structured as psycho-educational groups and include social interactional activities, role-playing, discussion, and didactic presentation. The focus is on sibling relationship skills, cognitions, and activities. During a total of 3 family nights, parents attend with their children. Part of the family night session involves parents and children together. Another part of the session involves parents being separated from children. Family Nights promote parents' understanding of sibling relationships, review concepts, provide strategies for parental support of siblings, and teach parents skills for dealing with sibling problems. Family Nights include dinner and last 2 hours.
Receives: Behavioral: SIBS Program
Contact-Equivalent Attention ControlPlacebo comparatorThe Contact-Equivalent Attention Control condition includes 12 weekly 90-minute afterschool group sessions for siblings led by two co-leaders. Students work on educational games and activities. Groups begin with an icebreaker and continue with games and projects. This condition also includes 3 family nights, where parents attend with their children. Activities of the Family Nights include children showing their parents the activities they have been engaging in during the sessions. Family Nights include dinner and last 2 hours. Part of the family night session involves parents and children together. Another part of the session involves parents being separated from children; during this part, parents will break out with one group leader, and siblings will work with the other group leader.
Receives: Behavioral: Control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Parenting of Siblings Measure

    The measure assesses parents' perceptions of three constructs: Parents' positive guidance, authoritarian control, and involvement (McHale et al., 2000; Updegraff et al., 2016). For each subscale, scores range from 1 to 5. Higher subscale scores indicate more positive guidance (i.e., better outcome), higher involvement (i.e., better outcome), and higher authoritarian control (i.e., worse outcome). Subscales are not combined into a total score.

    Measured: 16 weeks

  2. Sibling Prosocial Behavior

    The measure assesses parents' perceptions of one construct: Parents' ratings of children's supportive and prosocial behaviors (Stormshak, Bellanti, \& Bierman, 1996; Updegraff et al., 2016).

    Scores range from 1 to 6. Higher scores indicate parents' perceptions of target child's more prosocial behaviors toward their sibling (i.e., better outcome).

    Measured: 16 weeks

  3. Sibling Intimacy

    The measure assesses siblings' ratings of intimacy/emotional support (Blyth \& Foster-Clark, 1987). Scores range from 1 to 5. Higher scores indicate target child's perceptions of higher sibling intimacy and closeness (i.e., better outcome).

    Measured: 16 weeks

  4. Sibling Relationship Inventory: Negativity Subscale

    The measure assesses parents' ratings of sibling conflict and negativity (Stocker \& McHale, 1992). Scores range from 1 to 5. Higher scores indicate parents' perceptions of target child's greater negativity toward their sibling (i.e., worse outcome).

    Measured: 16 weeks

  5. Sibling Relationship Inventory: Negativity Subscale

    The measure assesses children's ratings of sibling conflict and negativity (Furman \& Buhrmester, 1985). Scores range from 1 to 5. Higher scores indicate target child's perceptions of higher sibling conflict and negativity (i.e., worse outcome).

    Measured: 16 weeks

Secondary outcomes (9)
  1. Self-efficacy Measure

    This measure assesses children's ratings of two constructs: social self-efficacy and emotional self-efficacy (Muris, 2001). For each subscale, scores range from 1 to 5. Higher subscale scores indicate greater social self-efficacy (i.e., better outcome) and greater emotional self-efficacy (i.e., better outcome). Subscales are not combined into a total score.

    Measured: 16 weeks

  2. Children's Depression Inventory

    This measure assesses children's ratings of their depressive symptoms (Kovacs, 1985). Items are scored on a scale from 0 to 2, and higher scores indicate greater depressive symptoms (i.e., worse outcome). If mean scores are used, scores range from 0 to 2. If sum scores are used, scores range from 0 to 52.

    Measured: 16 weeks

  3. Behavior Problem Index

    This measure assesses parents' perceptions of children's social emotional functioning in 6 domains (i.e., antisocial, anxious/depressed, headstrong, hyperactive, dependency, peer conflict; Peterson \& Zill, 1986). For all scales, items are scored on a scale from 1 to 3. For each subcale, higher scores indicate higher problem behavior in the domain (i.e., worse outcome). Mean scores are created for each subscale, and a total mean score is created across all domains - in all cases, higher scores indicate worse outcomes.

    Measured: 16 weeks

  4. Center for Epidemiological Depression Scale

    The CES-D (Radloff, 1977) assesses parents' depressive symptoms. Items are scored on a scale from 0 to 3, and higher scores indicate greater depressive symptoms (i.e., worse outcome). No subscales are created. If mean scores are used, scores range from 0 to 3. If sum scores are used, scores range from 0 to 60.

    Measured: 16 weeks

  5. Parenting Stress Index

    This measure assesses parents' perceptions of parental stress and includes two subscales: parental distress and dysfunctional interaction (Abidin, 1995). Items for each subscale are scored on a scale from 1 to 5. Mean scores can be created for each subscale, and higher scores indicate higher levels of distress (i.e., worse outcome) and higher dysfunctional interaction (i.e., worse outcome). A total scale score can be created across all items and higher scores indicate higher parenting stress (i.e., worse outcome).

    Measured: 16 weeks

  6. Children's Reports of Parental Behavior Inventory - Parent-Child Warmth

    This measure assesses parent and child's report of parent-child warmth (Schaefer, 1965). Items are scored on a scale of 1 to 5. Items are average and higher scores indicate greater perceptions of parent-child warmth (i.e., better outcome).

    Measured: 16 weeks

  7. Children's Reports of Parental Behavior Inventory - Harsh Discipline

    This measure assesses parent's reports of harsh discipline (Schaefer, 1965). Items are scored on a scale of 1 to 5. Items are average and higher scores indicate greater perceptions of harsh discipline (i.e., worse outcome).

    Measured: 16 weeks

  8. Parent-Child Conflict measure

    This measure assesses parents' perceptions of parent-child conflict (Smetana, 1988). Items are scored on a scale from 1 to 6. Average scores are created and higher values indicate greater parent-child conflict (i.e., worse outcome).

    Measured: 16 weeks

  9. Family Adaptability and Cohesion Evaluation Scales II

    This measure assesses parents' perceptions of family cohesion (Olson, Portner, \& Bell, 1982). Items are scored on a scale from 1 to 5. An average score is created and higher scores indicate greater family cohesion (i.e., better outcome).

    Measured: 16 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Oct 2018
  2. Study start29 Sep 2018
  3. Primary completion15 Dec 2025 (estimated)
  4. Study completion15 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized Controlled Trial involving a contact-equivalent control group
Masking
None (open label)
Enrolment
270 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03706014
Sponsor's protocol ID
SITE18-0185
Acronym
SIBS
Status last verified
Oct 2025
First submitted
26 Aug 2018
Last updated
27 Oct 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Updegraff KA, Umana-Taylor AJ, Rodriguez De Jesus SA, McHale SM, Feinberg MF, Kuo SI. Family-focused prevention with Latinos: What about sisters and brothers? J Fam Psychol. 2016 Aug;30(5):633-40. doi: 10.1037/fam0000200. Epub 2016 Apr 14.

    PubMed 27077238
  • Feinberg ME, Solmeyer AR, Hostetler ML, Sakuma KL, Jones D, McHale SM. Siblings are special: initial test of a new approach for preventing youth behavior problems. J Adolesc Health. 2013 Aug;53(2):166-73. doi: 10.1016/j.jadohealth.2012.10.004. Epub 2012 Nov 20.

    PubMed 23298985
  • Duran JG, Updegraff KA, Son D, Gallagher A, Umana-Taylor AJ, Feinberg ME. Trajectories and correlates of Latino/a children's sibling relationships. Dev Psychol. 2026 Jul 9:10.1037/dev0002227. doi: 10.1037/dev0002227. Online ahead of print.

    PubMed 42423725
  • Cahill KM, Updegraff KA, Umana-Taylor AJ, Feinberg ME. Engaging Latino Families in a Sibling-Focused Family Prevention Program. Prev Sci. 2026 Mar;27(3):376-389. doi: 10.1007/s11121-026-01886-3. Epub 2026 Apr 9.

    PubMed 41954835

Questions about this trial

What is this clinical trial studying?

A study testing SIBS Program in people with Promotion of Positive Sibling Relationships, run by Harvard University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 27 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Parenting of Siblings Measure (time frame: 16 weeks). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03706014, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Oct 2025.

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