- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04248036
Circle of Security - Parenting, COS-P
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
Status
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Zekiye Sag, BSc
- Phone Number: +46(0)317479671
- Email: zekiye.sag@vgregion.se
Study Contact Backup
- Name: Lena Nordeman, PhD
- Phone Number: +46(0)701714463
- Email: lena.nordeman@vgregion.se
Study Locations
-
-
Västra Götaland
-
Göteborg, Västra Götaland, Sweden
- Recruiting
- Psykologenheten för mödra- och barnhälsovården
-
Contact:
- Zekiye Sag, BSc
- Phone Number: 0733106567
- Email: zekiye.sag@vgregion.se
-
Contact:
- Zekiye Sag, BSc
- Phone Number: 0317479671
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
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
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.
|
|
Through study completion, an average of 1 year.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Zekiye Sag, BSc, Regionhälsan, Region Västra Götaland
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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