Social Intelligence Training for Custodial Grandfamilies
Social Intelligence Training for Custodial Grandmothers and Their Adolescent Grandchildren
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Phase
Phase
- Phase 2
Contacts and Locations
Study Contact
Study Contact
- Name: Gregory C Smith, EdD
- Phone Number: 330 672-9993
- Email: gsmith2@kent.edu
Study Locations
-
-
Ohio
-
Kent, Ohio, United States, 44242
- Recruiting
- Kent State University
-
Contact:
- Gregory C Smith, EdD
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Grandmothers of any age or race
- Providing full-time care to an adolescent grandchild between ages 12-18
- Providing care in their own residence
- Providing care in total absence of the grandchild's biological parents.
- The target adolescent custodial grandchild will be of either gender
- Between ages 12- 18
- The custodial grandmother has provided full-time care for at least 6 months in total absence of the biological parents.
- Understanding of English well enough to comprehend all study materials.
Exclusion Criteria:
* Cognitive or behavioral problems that limit the ability of grandmothers and grandchildren to comprehend the intervention and complete study measures
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
EXPERIMENTAL: Online Social Intelligence Training
The Social Intelligence Intervention (SII) is delivered online to both custodial grandmothers and their adolescent grandchild separately.
This is the sole active treatment condition within this RCT.
|
The SII consists of short 5-10 minute sessions organized into 7 modules designed to raise awareness of human nature and social relationships.
The approach is based on evidence that SII is best advanced through interventions that modify key social cognitions regarding social engagement and enhance efficacy expectations regarding performance in social situations.
|
|
PLACEBO_COMPARATOR: Attention Control (AC)
The attention control (AC) condition, known as The Healthy Living program provides information about different aspects of health.
|
A placebo condition delivered online to both custodial grandmothers and their adolescent grandchild which presents health-related information only.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Composite Latent Construct "Social Sensitivity"
Time Frame: Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention.
|
Measured by four standardized instruments self-report scales and daily diary entries
|
Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention.
|
|
Change in Composite Latent Construct "Openness to Others"
Time Frame: Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
Measured by two standardized self-report scales
|
Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
|
Change in Composite Latent Construct "Social Self-Confidence"
Time Frame: Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
Measured by three standardized self-report instruments
|
Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
|
Change in Composite Latent Construct "Relationships and Social Ties"
Time Frame: Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
Measures of ambivalence, close relationships, positive family connections, relationships with important groups; and social connections with peers.
|
Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
|
Change in Physical Health
Time Frame: Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
Self-reported health status measured by the Sf-12 Survey
|
Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
|
Change in Composite Latent Construct "Psychological and Emotional Well-Being"
Time Frame: Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
Separate measures of self-esteem, loneliness, depression, anxiety, introversion-extroversion, affective reactivity, social resilience
|
Change will be assessed from baseline immediately post intervention, as well as at 3, 6, and 9 months post intervention
|
Other Outcome Measures
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Open Ended Interviews
Time Frame: Within one month after completing the social intelligence intervention.
|
To be created open-ended measure of treatment satisfaction
|
Within one month after completing the social intelligence intervention.
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Gregory C Smith, EdD, Kent State University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Study Start
Primary Completion (ANTICIPATED)
Primary Completion
Study Completion (ANTICIPATED)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (ACTUAL)
First Posted
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- GCSmith RCT NIA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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