Intensive Parent-child Interaction Therapy (I-PCIT): Feasibility and Effectiveness Study.

Overview

About this study

The purpose of this study is to evaluate the feasibility of implementing I-PCIT in a community clinic, measured by treatment attendance and caregiver’s satisfaction compared to the current gold-standard of PCIT-au.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Participants in I-PCIT will be enrolled from the outpatient Behavioral Health Clinic in La Crosse WI. PCIT-au group will be a chart review from La Corsse WI and Rochester MN.
Children, ages 2-7 years old.
Children whose measure of EBP rated above the clinically significant range (T-score ≥ 60) on ECBI.
Eligible families will have to commit to a full course of treatment.
Patients who have answered yes to research authorization.
Children of patients who have answered yes to research authorization.

Exclusion Criteria:

Children with an intellectual disability, Autistic Disorder, or a psychotic disorder.
The inability of parents to attend sessions daily.
Patients that answered no to research authorization

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
La Crosse, Wis. Mayo Clinic principal investigator Chelsea Ale, Ph.D., L.P.	Closed for enrollment

Mayo Clinic Location

Status

La Crosse, Wis.

Mayo Clinic principal investigator

Chelsea Ale, Ph.D., L.P.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials