Skip to content

Developmental Pilot of Support Groups for Caregivers of Children With DLD

Developmental Pilot of Support Groups for Caregivers of Children With DLD

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07536217
Enrollment
15
Registered
2026-04-17
Start date
2026-02-20
Completion date
2026-06-15
Last updated
2026-04-17

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

Conditions

Developmental Language Disorder

Keywords

Support Groups, Developmental Language Disorder, EPIS, Implementation Science, Peer Support

Brief summary

The purpose of this study is to test a new support group curriculum that we designed to support parents of children with Developmental Language Disorder (DLD).

Detailed description

After completing the informed consent process and eligibility has been verified, participants will complete parenting questionnaires. They will then be asked to attend 8-10 weekly support group meetings with other participants. Support group meetings are held remotely. After each meeting, participants will be asked to complete a brief questionnaire to learn about their experiences. After the final support group meeting, participants will be asked to complete the same parenting questionnaires as at study initiation. Participants will also be asked to complete a focus group with other support group attendees to share about their experiences in the group.

Interventions

BEHAVIORALSupport Groups

A manualized support group for families who care for a child with developmental language disorder (DLD)

Sponsors

University of Delaware
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Caregiver of an elementary aged (5-12 year old) child with a lab-confirmed diagnosis of DLD

Exclusion criteria

* Not able to participate via teletherapy in a support group delivered in English.

Design outcomes

Primary

MeasureTime frameDescription
Qualitative interviews with participantsup to 2 weeks after interventionFocus group and/or one-on-one interviews with support group participants

Secondary

MeasureTime frameDescription
Survey on Knowledge Seeking Behaviorsup to 4 weeks before and 2 weeks after interventionWe will use a survey developed by Darefsky (2022, adapted from (Al-Daihani \& Al-Ateeqi, 2015). The survey consists of 9 total questions, of which there are two yes/no items, two multiple choice items, and four Likert scale items. This measure is not scored in a way that results in minimum or maximum scores, or outcomes. This measure is used to collect descriptive information about types and sources of information that caregivers desire in relation to their child's diagnosis.
Child Adjustment and Parent Efficacy Scaleup to 4 weeks before and 2 weeks after interventionThe Child Adjustment and Parent Efficacy Scale (CAPES; Morawska \& Sanders, 2010) includes 50 Likert scale items This yields two measurements: one for Child Emotional and Behavioral Problems and one for Parent Efficacy. Child Emotional and Behavioral Problems: Minimum score = 0; Maximum score = 81. Higher scores indicate greater levels of child problems. Parent Efficacy: Minimum score = 19; Maximum score = 190 Higher scores indicate greater levels of parent self-efficacy.
Parenting Stress Index, Fourth Edition Short Formup to 4 weeks before and 2 weeks after interventionThe Parenting Stress Index, Fourth Edition Short Form (PSI-4-SF; Abidin, 2012)includes 36 items. Minimum score = 36; Maximum score = 180. Higher scores indicate higher parent stress levels.
Family Support Scaleup to 4 weeks before and 2 weeks after interventionThe Family Support Scale (FSS; Dunst, et al., 1984)includes 18 Likert scale items. Minimum score = 0 Maximum score = 95 Higher scores indicate more family support.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAmanda Van Horne, PhD

University of Delaware

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026