Circle of Security - Parenting, COS-P

November 5, 2021 updated by: Vastra Gotaland Region

Trygghetscirkelns föräldraskap (Circle of Security - Parenting) - Gruppintervention för föräldrar Med Barn förskoleåldern - En Pilotstudie.

Background: Circle of Security-Parenting is a parental support program that provides basic knowledge about the emotional needs of children up to 6 years old and is illustrated graphically based on a circle model. It is designed to be given in group and includes 8 sessions of 90 minutes each.

COS-P is regularly offered as a parent support intervention within the Psychology units for Maternal and Child health care in Södra Älvsborg and Fyrbodal with the aim of increasing the quality of the parent-child relationship.

Objective: Prior to a planned RCT study, clarify which inclusion criterias are used for the COS-P intervention within the two psychology units, which parents accept and complete the study and investigate change in self-assessed depression, anxiety and stress level in the parent, the parent's reflective ability and symptoms in the child estimated by the parent.

Method: The parents who participate in the planned COS-P groups within the two units in spring/autumn of 2020 will fill in surveys before group start, at the end of intervention and 6-months follow up. Change between baseline and posttest as well as between baseline and 6-month follow-up will be analyzed.

The psychologists will fill in specially formulated questionnaires regarding their inclusion criterias.

Expected result: This pilot study is expected to describe the group of parents receiving COS-P and the inclusion criterias for the intervention used by the psychologists in the Psychology units for Maternal and Child health care in Södra Älvsborg and Fyrbodal.

Study Overview

Detailed Description

Background: Circle of Security-Parenting (COS-P) is a manual-based, psychoeducational parental support program that includes 8 group sessions of 90 minutes each. It provides basic knowledge about the emotional needs of children up to 6 years old and how parents can meet those needs to promote secure attachment in their child.

COS-P is a parental support groupintervention that is regularly given in the Psychology units for Maternal and Child health care in Södra Älvsborg and Fyrbodal and has become an appreciated intervention by both the participants and the psychologists who lead the groups. The method is also increasingly used both in Sweden and internationally but the systematic evaluation of COS-P is at the same time very limited. It is also unclear what the inclusion criterias and outcome measures are for COS-P in the Psychology unit for Maternal and Child health care.

Objective: The purpose of this pilot study is to provide knowledge of the inclusion criterias and outcome measures for COS-P within the Psychological units for Maternal and Child health care in Södra Älvsborg and Fyrbodal before more research subjects and activities are included in a randomized controlled study. The study also aims to examine change in the participating parents between baseline and posttest as well as the 6-month follow-up regarding self-assessed depression, anxiety and stress level, the parent's reflective ability and symptoms in the child estimated by the parent.

Additionally, the study will describe whether there is a relationship between demographic data and self-assessed depression, anxiety, stress level, the parent's reflective ability and symptoms of the child estimated by the parent at baseline and posttest and at baseline and 6-month follow-up.

Method: The parents who are assessed suitable for COS-P and accept to participate in the pilot study during spring/autumn 2020 will fill in surveys before group start, after completion and at the 6-month follow-up. In total, 50 parents will be included in the study.

Psychologists will fill in specially formulated questionnaires regarding their inclusion criterias.

Expected result: This pilot study is expected to describe the group of parents receiving COS-P and the inclusion criterias for the intervention used by the psychologists in the Psychology units for Maternal and Child health care in Södra Älvsborg and Fyrbodal.

Study Type

Interventional

Enrollment (Anticipated)

50

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 Contact

Study Contact Backup

Study Locations

    • Västra Götaland
      • Göteborg, Västra Götaland, Sweden
        • Recruiting
        • Psykologenheten för mödra- och barnhälsovården
        • Contact:
        • Contact:
          • Zekiye Sag, BSc
          • Phone Number: 0317479671

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
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion criteria:

  • The parent has difficulties in understanding and/or reflecting upon the childs signals/emotional needs.
  • The parent has diffuculties in bonding to the child.
  • The parent has difficulties in helping the child with emotional regulation.

Exclusion criteria:

  • Serious mental illness
  • Lack of language skills in Swedish.

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Circle Of Security Parenting, COS-P
Pilot study, assessing eligibility, outcome measures and compliance to Group intervention
Circle of Security - Parenting is a manual-based, psychoeducational intervention program in group that includes 8 group sessions of 90 minutes each.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short term effect of COS-P on parental reflective functioning.
Time Frame: Change from baseline to completion of intervention, an average of 8-12 weeks.
What is the effect of COS-P on the parent´s capacity to reflect upon both his/her own internal mental experiences and those of the child measured by change in scores in "The Parental Reflective Functioning Questionnaire", the 18 items version, from baseline to posttest?
Change from baseline to completion of intervention, an average of 8-12 weeks.
Short term effect of parent´s participation in COS-P on the child´s behavioral problems/mental health.
Time Frame: Change from baseline to completion of intervention, an average of 8-12 weeks.
What is the effect of the parent´s participation in COS-P on the child´s behavioral problems/mental health measured by change in scores in "The Strengths and Difficulties Questionnaire (SDQ) for preschool Children" from baseline to posttest..
Change from baseline to completion of intervention, an average of 8-12 weeks.
Long term effect of COS-P on parental reflective functioning.
Time Frame: Change from baseline to 6-month follow-up.
What is the effect of COS-P on the parent´s capacity to reflect upon both his/her own internal mental experiences and those of the child measured by change in scores in "The Parental Reflective Functioning Questionnaire", the 18 items version, from baseline to 6-month follow-up?
Change from baseline to 6-month follow-up.
Long term effect of parent´s participation in COS-P on the child´s behavioral problems/mental health.
Time Frame: Change from baseline to 6-month follow-up.
What is the effect of the parent´s participation in COS-P on the child´s behavioral problems/mental health measured by change in scores in "The Strengths and Difficulties Questionnaire (SDQ) for preschool Children" from baseline to 6-month follow-up?
Change from baseline to 6-month follow-up.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short term effect of COS-P on parental stress level.
Time Frame: Change from baseline to completion of intervention, an average of 8-12 weeks.
What is the effect of COS-P on parental stress level measured by change in scores in "Swedish Parenthood Stress Questionnaire" from baseline to posttest?
Change from baseline to completion of intervention, an average of 8-12 weeks.
Short term effect of COS-P on depressive mood in parent.
Time Frame: Change from baseline to completion of intervention, an average of 8-12 weeks.
What is the effect of COS-P on depressive mood in parent measured by change in scores in "Beck Depressive Inventory - 2" from baseline to posttest?
Change from baseline to completion of intervention, an average of 8-12 weeks.
Short term effect of COS-P on anxiety in parent.
Time Frame: Change from baseline to completion of intervention, an average of 8-12 weeks.
What is the effect of COS-P on anxiety in parent measured by change in scores in "Beck Anxiety Inventory" from baseline to posttest?
Change from baseline to completion of intervention, an average of 8-12 weeks.
Long term effect of COS-P on parental stress level.
Time Frame: Change from baseline to 6-month follow-up.
What is the effect of COS-P on parental stress level measured by change in scores in "Swedish Parenthood Stress Questionnaire"?
Change from baseline to 6-month follow-up.
Long term effect of COS-P on depressive mood in parent.
Time Frame: Change from baseline to 6-month follow-up.
What is the effect of COS-P on depressive mood in parent measured by change in scores in "Beck Depressive Inventory - 2" from baseline to 6-month follow-up?
Change from baseline to 6-month follow-up.
Long term effect of COS-P on anxiety in parent.
Time Frame: Change from baseline to 6-month follow-up.
What is the effect of COS-P on anxiety in parent measured by change in scores in "Beck Anxiety Inventory" from baseline to 6-month follow-up?
Change from baseline to 6-month follow-up.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
A questionnaire designed for the psychologists in the study containing 4 specific questions.
Time Frame: Through study completion, an average of 1 year.
  1. "What inclusion criterias did you use when you offered a parent to participate in COS-P?"
  2. "How many parents have you offered the opportunity to participate in COS-P over the past 6 months?"
  3. "How many of these have accepted to participate in COS-P?"
  4. "What other intervention have you offered to those parents who have declined to participate in COS-P?"
Through study completion, an average of 1 year.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Zekiye Sag, BSc, Regionhälsan, Region Västra Götaland

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)

June 30, 2020

Primary Completion (Anticipated)

December 31, 2022

Study Completion (Anticipated)

December 31, 2022

Study Registration Dates

First Submitted

January 19, 2020

First Submitted That Met QC Criteria

January 29, 2020

First Posted (Actual)

January 30, 2020

Study Record Updates

Last Update Posted (Actual)

November 15, 2021

Last Update Submitted That Met QC Criteria

November 5, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • VGFOUSA-903421

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.

Clinical Trials on Parenting

Clinical Trials on Circle of Security - Parenting, COS-P

Subscribe