- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07168460
- Original Trial
Social Working Dogs Support to Children With Problematic School Absence
Social Working Dogs Support To Children With Problematic School Absence
The purpose of this project is to investigate whether trained social service dogs can increase students' school attendance and school motivation, and ultimately contribute to students reaching the basic learning goals. Main research questions are:
- What are the effectiveness and cost-effectiveness of having social service dogs support at schools to improve learning outcome and school attendance in students with problematic school absence?
- What are the risks to the health and well-being of those social working dogs when they work in the school environment as well as the challenges in bringing dogs to the schools?
Researchers compared the intervention group which consisted of students supported by social working dogs, to the control group of students supported by special education teachers. Participants were assigned to each group randomly. Students from each group met the support teams for 30 minutes per session, twice per week for 10-12 weeks. During the intervention, children had physical contact with dogs as much as they wished and on consideration of dogs' welfare. The dog handler carried out some pedagogical tasks, such as children reading to the dog while the dog was next to the child or when its head was on the child's lap. The dog handlers documented the process of each session and observed the children on their educational tasks. Children in the control group met special education teachers and received pedagogical tasks involving Swedish, mathematics, etc. Similar to the dog team, special education teachers documented the process and observed the performance of children's educational tasks.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Uppsala, Sweden
- Uppsala University & Swedish University of Agricultural Sciences
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children from grades 3-9 with at least 15% absence from school during at least one semester and receiving no additional support.
Exclusion Criteria:
- Children who had 50%-100% absenteeism for more than a year
- Children who were severely allergic to dogs or who had previous negative experiences with dogs
- Children from grades 1-3
- Children who had previously participated in an intervention with a social working dog.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Social working dogs team
Children are randomized to this social working dogs team to receive dog-assisted educational tasks such as reading.
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Children in the intervention group received dog-assisted support for 30 minutes per session, twice per week for 10-12 weeks.
The process began with children meeting school dog with dog handlers either at their home or at school.
During the intervention, children had physical contact with dogs as much as they wished and on consideration of dogs' welfare.
The dog handler carried out some pedagogical tasks, such as children reading to the dog while the dog was next to the child or when its head was on the child's lap.
The dog handler documented the process of each session in a protocol filled in after each session and observed the children on their educational tasks.
|
|
Active Comparator: Special education teachers team
Children are randomized to this active control group to perform educational tasks with the support of special educational teachers.
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Children in the control group met special education teachers and received pedagogical tasks involving Swedish, mathematics, etc.
Similar to the dog team, special education teachers documented the process and observed the performance of children's educational tasks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
School absenteeism
Time Frame: T0-The whole semester before intervention (5 months pre-intervention), T1-The whole semester during intervention (5 months during intervention), and T2 - The whole semester after intervention (5 months after intervention).
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Children's weekly school attendance (%) were retrieved from school registration records on children's attendance.
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T0-The whole semester before intervention (5 months pre-intervention), T1-The whole semester during intervention (5 months during intervention), and T2 - The whole semester after intervention (5 months after intervention).
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Learning achievement
Time Frame: T0-The whole semester before intervention (5 months pre-intervention), T1-The whole semester during intervention (5 months during intervention), and T2 - The whole semester after intervention (5 months after intervention).
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Children's attainment of basic learning goals was measured through grades obtained on two subjects: Swedish and Mathematics.
Children were graded as pass (Godkänd) or fail (Undergodkänd) in Swedish and Mathematics.
Data were retrieved through school reports.
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T0-The whole semester before intervention (5 months pre-intervention), T1-The whole semester during intervention (5 months during intervention), and T2 - The whole semester after intervention (5 months after intervention).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Children's health-rated quality of life (HRQOL)
Time Frame: T0 - pre-intervention, T1 - immediately post intervention, T2 - 3 months post intervention, and T3 - 6 months post intervention
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Children's health-rated quality of life (HRQOL) of both control and intervention classes was measured using the Child Health Utility 9 Dimensions (CHU9D), a generic preference-based HRQOL measure for use in children and youth.
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T0 - pre-intervention, T1 - immediately post intervention, T2 - 3 months post intervention, and T3 - 6 months post intervention
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lena Lidfors, Doctorate in Ethology, Swedish University of Agricultural Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2022-01706-01
- N2021-0022 (Other Grant/Funding Number: Agria/SKK research fund)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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