Social Working Dogs Support to Children With Problematic School Absence

September 9, 2025 updated by: Uppsala University

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:

  1. 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?
  2. 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

Detailed Description

The aim of this project is to investigate whether an intervention delivered by trained social working dog teams can increase school attendance among school-age children in grades 3-9, contribute to children achieving the basic learning goals, and improve health-related quality of life. The study design is an individually-randomized controlled trial with two arms - intervention and control. Randomization is conducted at the individual level within each school through lottery. Schools in Sweden were contacted by sending out flyers. Principals who wanted their schools to participate in the project contacted the project manager. The selection criteria for inclusion in the project are children from grades 3-9 with at least 15% absence from school during at least one semester, receiving no additional support.The criteria for exclusion are as follows: 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; and children from grades 1-3. Additionally, children who had previously participated in an intervention with a social working dog were excluded, as the potential impact on the results is unknown. Participation was voluntary, and written consent forms from both children and parents/ guardians were obtained. The study population includes school-age children from grades 3-9 in Sweden. A sample size of around 64 school-going children with a 1:1 allocation was allocated within the schools into control and intervention groups. Primary outcome data were collected at the following time points: T0 - pre-intervention (the whole semester before intervention), T1 - the whole semester during intervention, and T2 - the whole semester after intervention. Secondary outcome data were collected at T0 - pre-intervention, T1 - immediately post intervention, T2 - 3 months post intervention, and T3 - 6 months post intervention.

Study Type

Interventional

Enrollment (Actual)

64

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Uppsala, Sweden
        • Uppsala University & Swedish University of Agricultural Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
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.
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).
Children's weekly school attendance (%) were retrieved from school registration records on children's attendance.
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).
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).
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.
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
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.
T0 - pre-intervention, T1 - immediately post intervention, T2 - 3 months post intervention, and T3 - 6 months post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lena Lidfors, Doctorate in Ethology, Swedish University of Agricultural Sciences

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 13, 2022

Primary Completion (Actual)

February 14, 2024

Study Completion (Actual)

February 14, 2024

Study Registration Dates

First Submitted

September 1, 2025

First Submitted That Met QC Criteria

September 9, 2025

First Posted (Estimated)

September 11, 2025

Study Record Updates

Last Update Posted (Estimated)

September 11, 2025

Last Update Submitted That Met QC Criteria

September 9, 2025

Last Verified

September 1, 2025

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)?

UNDECIDED

IPD Plan Description

IDP sharing plan has not been decided as they are sensitive data, and that we need approval from our university GDPR and legal department to do so.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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