Integrated Maternal Psychosocial Assessment to Care Trial (IMPACT) Full Trial
Primary Purpose
Anxiety, Depression
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Cognitive Behavioral Therapy
Sponsored by

About this trial
This is an interventional treatment trial for Anxiety focused on measuring Anxiety, Depression, CBT
Eligibility Criteria
Inclusion criteria:
Pregnant women will be eligible for Phase 2 if they are:
- < 28 weeks gestation (to provide the opportunity to complete 6 modules and follow-up questionnaires prior to delivery)
- able to speak/read English; and (3) willing to complete email questionnaires
Exclusion Criteria:
- >28 weeks gestation
- unable to speak/read English
- unable to complete email questionnaires
Sites / Locations
- Westview Health Centre
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Screening and CBT
Usual care
Arm Description
Screening and Cognitive Behavioral Therapy. The intervention group will be screened and if they need criteria they will complete the 6, 30-minute online, interactive CBT modules over 6 weeks.
Usual prenatal care
Outcomes
Primary Outcome Measures
The primary outcome of this study is the feasibility/acceptability of integrated psychosocial care and its components.
Feasibility/acceptability of the intervention will be assessed through individual face-to-face or telephone-based semi-structured qualitative interviews of both clinic staff and women in the intervention group. The field does not allow for all questions to be provided. Sample question for clinic staff is 'What aspects made it easy/challenging to use the tablet for prenatal assessment as part of routine prenatal care?' Sample questions for intervention group participants: 1)How did you feel about answering these kinds of questions on a tablet?; 2)Please describe any concerns you had about answering these questions on a tablet; 3)How would you prefer the results to be shared with you
Secondary Outcome Measures
Maternal depression, anxiety, stress
Depression, Anxiety, and Stress Scale (DASS-21) Self-reported by mother on emailed questionnaire
Maternal coping
The Brief Cope Self-reported by mother on emailed questionnaire
Relationship Adjustment
Scale: Dyadic Adjustment Scale, DAS-7 Self-reported by mother on emailed questionnaire
Parenting Stress
Parenting Stress Scale Self-reported by mother
Parenting competence
Parenting Sense of Competence Scale Self-reported by mother on emailed questionnaire
Maternal-infant attachment
Maternal Attachment Inventory (MAI) Self-reported by mother on emailed questionnaire
Trait anxiety
State Trait Anxiety Inventory (STAI) Self-reported by mother on emailed questionnaire
Full Information
NCT ID
NCT01901796
First Posted
July 10, 2013
Last Updated
November 11, 2019
Sponsor
University of Calgary
Collaborators
Norlien Foundation, Women and Children's Health Research Institute, Canada
1. Study Identification
Unique Protocol Identification Number
NCT01901796
Brief Title
Integrated Maternal Psychosocial Assessment to Care Trial (IMPACT) Full Trial
Official Title
Integrated Maternal Psychosocial Assessment to Care Trial (IMPACT): Intervening Early to Improve Maternal and Family Well-being.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2014 (undefined)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
Norlien Foundation, Women and Children's Health Research Institute, Canada
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
We hypothesize that the intervention will: (1) offer a feasible approach for providing mental healthcare to pregnant women and have a high level of acceptability by pregnant women and healthcare providers; (2) reduce symptoms of depression, stress, anxiety, and parenting stress; improve parenting competence, coping, and relationship adjustment compared to usual care; and (3) reduce the risk of poor maternal-infant attachment. As such, this early intervention holds promise for reducing maternal mental health morbidity and its negative influences on infants, children, and families.
Detailed Description
One of the main reasons that women do not receive treatment is that their mood and anxiety problems are not detected. Despite recommendations and high rates of acceptance by providers and women, only a minority of providers conduct psychosocial assessments as part of routine prenatal care. Computer-based 'screening' is an acceptable and feasible approach to assessment of sensitive issues including prenatal and postnatal intimate partner violence, mental health problems, and postpartum depression by patients and providers. It is well-suited for busy clinical settings and is advantageous in that it offers a consistent approach to assessment, is resource-sparing, can be tailored to meet the specific needs of patients, can be used with audio/video for low literacy, provides a real-time summary for patients/providers,achieves similar or higher rates of disclosure of violence and mental health problems, and is preferred by patients because they perceive it as more anonymous compared to interviews or questionnaires.
However, psychosocial assessment on its own is ineffective in preventing or treating mood disorders and unethical in the absence of treatment options. As such, many providers do not assess pregnant women for mood disorders because non-pharmacological treatments are frequently unavailable and pregnant women prefer them. Cognitive behavioural therapy (CBT) is a highly effective, non-pharmacological treatment for depression and anxiety and is recommended by perinatal national Australian guidelines as a potentially effective EARLY intervention for reducing the risk of maternal-child outcomes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Depression
Keywords
Anxiety, Depression, CBT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
5000 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Screening and CBT
Arm Type
Experimental
Arm Description
Screening and Cognitive Behavioral Therapy. The intervention group will be screened and if they need criteria they will complete the 6, 30-minute online, interactive CBT modules over 6 weeks.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Usual prenatal care
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavioral Therapy
Intervention Description
Cognitive Behavioral Therapy- an effective, non-pharmacological treatment for depression and anxiety.
Primary Outcome Measure Information:
Title
The primary outcome of this study is the feasibility/acceptability of integrated psychosocial care and its components.
Description
Feasibility/acceptability of the intervention will be assessed through individual face-to-face or telephone-based semi-structured qualitative interviews of both clinic staff and women in the intervention group. The field does not allow for all questions to be provided. Sample question for clinic staff is 'What aspects made it easy/challenging to use the tablet for prenatal assessment as part of routine prenatal care?' Sample questions for intervention group participants: 1)How did you feel about answering these kinds of questions on a tablet?; 2)Please describe any concerns you had about answering these questions on a tablet; 3)How would you prefer the results to be shared with you
Time Frame
6 weeks post randomization
Secondary Outcome Measure Information:
Title
Maternal depression, anxiety, stress
Description
Depression, Anxiety, and Stress Scale (DASS-21) Self-reported by mother on emailed questionnaire
Time Frame
on recruitment, 6 weeks post randomization and 3 months postpartum
Title
Maternal coping
Description
The Brief Cope Self-reported by mother on emailed questionnaire
Time Frame
on recruitment, 6 weeks post-randomization and 3 months postpartum
Title
Relationship Adjustment
Description
Scale: Dyadic Adjustment Scale, DAS-7 Self-reported by mother on emailed questionnaire
Time Frame
on recruitment, 6 weeks post-randomization and 3 months postpartum
Title
Parenting Stress
Description
Parenting Stress Scale Self-reported by mother
Time Frame
3 months postpartum
Title
Parenting competence
Description
Parenting Sense of Competence Scale Self-reported by mother on emailed questionnaire
Time Frame
3 months postpartum
Title
Maternal-infant attachment
Description
Maternal Attachment Inventory (MAI) Self-reported by mother on emailed questionnaire
Time Frame
3 months postpartum
Title
Trait anxiety
Description
State Trait Anxiety Inventory (STAI) Self-reported by mother on emailed questionnaire
Time Frame
on recruitment, 6 weeks postrandomization, 3 months postpartum
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria:
Pregnant women will be eligible for Phase 2 if they are:
< 28 weeks gestation (to provide the opportunity to complete 6 modules and follow-up questionnaires prior to delivery)
able to speak/read English; and (3) willing to complete email questionnaires
Exclusion Criteria:
>28 weeks gestation
unable to speak/read English
unable to complete email questionnaires
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dawn A Kingston, Ph.D
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Westview Health Centre
City
Stony Plain
State/Province
Alberta
ZIP/Postal Code
T7Z 2M7
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
35687403
Citation
Bright KS, Stuart S, Mcneil DA, Murray L, Kingston DE. Feasibility and Acceptability of Internet-Based Interpersonal Psychotherapy for Stress, Anxiety, and Depression in Prenatal Women: Thematic Analysis. JMIR Form Res. 2022 Jun 10;6(6):e23879. doi: 10.2196/23879.
Results Reference
derived
PubMed Identifier
31888712
Citation
Bright KS, Mughal MK, Wajid A, Lane-Smith M, Murray L, Roy N, Van Zanten SV, Mcneil DA, Stuart S, Kingston D. Internet-based interpersonal psychotherapy for stress, anxiety, and depression in prenatal women: study protocol for a pilot randomized controlled trial. Trials. 2019 Dec 30;20(1):814. doi: 10.1186/s13063-019-3897-z.
Results Reference
derived
PubMed Identifier
24597683
Citation
Kingston D, Austin MP, Hegadoren K, McDonald S, Lasiuk G, McDonald S, Heaman M, Biringer A, Sword W, Giallo R, Patel T, Lane-Smith M, van Zanten SV. Study protocol for a randomized, controlled, superiority trial comparing the clinical and cost- effectiveness of integrated online mental health assessment-referral-care in pregnancy to usual prenatal care on prenatal and postnatal mental health and infant health and development: the Integrated Maternal Psychosocial Assessment to Care Trial (IMPACT). Trials. 2014 Mar 6;15:72. doi: 10.1186/1745-6215-15-72.
Results Reference
derived
Learn more about this trial
Integrated Maternal Psychosocial Assessment to Care Trial (IMPACT) Full Trial
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