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Behavioral Intervention
PHM™ Pathway for Parent Mental Health
N/A
Waitlist Available
Led By Anne C McKechnie, PhD, RN
Research Sponsored by University of Minnesota
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks after birth
Awards & highlights
Summary
This trial will test a new intervention pathway designed to help lower psychological distress and improve caregiving skills for parents after a major fetal anomaly diagnosis.
Eligible Conditions
- Parent Mental Health
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 weeks after birth
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks after birth
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Center for Epidemiology Scale-Depression (CES-D) score
Change in Impact of Event Scale score
Change in State-Trait Anxiety Inventory score
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention (PHM)Experimental Treatment1 Intervention
This pathway is intended to be a tool to enhance support for a mother/birthing person and her caregiving partner, facilitate communication with healthcare providers, and promote development of caregiving to optimize maternal-fetal, infant, and family health.
Group II: Usual Care Group (UC)Active Control1 Intervention
The control group participants will receive care as usual.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
PHM™ Pathway
2020
N/A
~60
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Who is running the clinical trial?
University of MinnesotaLead Sponsor
1,395 Previous Clinical Trials
1,553,268 Total Patients Enrolled
Anne C McKechnie, PhD, RNPrincipal InvestigatorUniversity of Minnesota
1 Previous Clinical Trials
23 Total Patients Enrolled
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