Trial Outcomes & Findings for Parenting Support for Justice Involved Families (NCT NCT06329336)

Last Updated: 2026-05-20

Results Overview

Questionnaire measuring parental warmth and consistency, scores range from 0 to 4, high scores reflect higher warmth and consistency.

Recruitment status

COMPLETED

Study phase

Target enrollment

13 participants

Primary outcome timeframe

Pretest assessments were conducted 2-3 weeks prior to the start of the 6-week program, and posttest assessments were conducted within 2-3 weeks of completion of the program.

Results posted on

2026-05-20

Participant Flow

Our community partner serving justice system involved families facilitated the invitation of parents with lived experience re-entering the community to participate in the parenting intervention via word of mouth and flyers distributed by community partners. Thirteen participants were enrolled into the research study.

Participant milestones

Participant milestones
Measure	Intervention Parents who participated in the intervention
Overall Study STARTED	13
Overall Study COMPLETED	13
Overall Study NOT COMPLETED	0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Parenting Support for Justice Involved Families

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure	Intervention n=13 Participants Parents who participated in the intervention
Age, Continuous	32.18 Years STANDARD_DEVIATION 9.18 • n=30 Participants
Sex: Female, Male Female	10 Participants n=30 Participants
Sex: Female, Male Male	3 Participants n=30 Participants
Race (NIH/OMB) American Indian or Alaska Native	1 Participants n=30 Participants
Race (NIH/OMB) Asian	0 Participants n=30 Participants
Race (NIH/OMB) Native Hawaiian or Other Pacific Islander	0 Participants n=30 Participants
Race (NIH/OMB) Black or African American	6 Participants n=30 Participants
Race (NIH/OMB) White	3 Participants n=30 Participants
Race (NIH/OMB) More than one race	0 Participants n=30 Participants
Race (NIH/OMB) Unknown or Not Reported	3 Participants n=30 Participants
Ethnicity (NIH/OMB) Hispanic or Latino	1 Participants n=30 Participants
Ethnicity (NIH/OMB) Not Hispanic or Latino	10 Participants n=30 Participants
Ethnicity (NIH/OMB) Unknown or Not Reported	2 Participants n=30 Participants
Region of Enrollment United States	13 Participants n=30 Participants

PRIMARY outcome

Timeframe: Pretest assessments were conducted 2-3 weeks prior to the start of the 6-week program, and posttest assessments were conducted within 2-3 weeks of completion of the program.

Questionnaire measuring parental warmth and consistency, scores range from 0 to 4, high scores reflect higher warmth and consistency.

Outcome measures

Outcome measures
Measure	Intervention n=13 Participants Participants in the Intervention
Parenting Behavior Inventory - Very Short Form Pretest	3.42 Units on a Scale Standard Deviation 0.68
Parenting Behavior Inventory - Very Short Form Posttest	3.36 Units on a Scale Standard Deviation 1.10

PRIMARY outcome

Timeframe: Pretest assessments were conducted 2-3 weeks prior to the start of the 6-week program, and posttest assessments were conducted within 2-3 weeks of completion of the program.

Questionnaire measuring mental health - Depressive symptoms, scores range from 0 to 27, higher scores indicate a greater number or severity of depressive symptoms

Outcome measures

Outcome measures
Measure	Intervention n=13 Participants Participants in the Intervention
PHQ-9 Depressive Symptoms Pretest	6.23 Units on a Scale Standard Deviation 4.88
PHQ-9 Depressive Symptoms Posttest	3.00 Units on a Scale Standard Deviation 3.47

PRIMARY outcome

Timeframe: Pretest assessments were conducted 2-3 weeks prior to the start of the 6-week program, and posttest assessments were conducted within 2-3 weeks of completion of the program.

Questionnaire measuring mental health - Anxiety Symptoms, scores range from 0 to 21, higher scores indicated a greater number of severity of anxiety symptoms

Outcome measures

Outcome measures
Measure	Intervention n=13 Participants Participants in the Intervention
GAD-7 Anxiety Symptoms Pretest	4.64 Units on a Scale Standard Deviation 4.47
GAD-7 Anxiety Symptoms Posttest	3.69 Units on a Scale Standard Deviation 3.64

Adverse Events

Intervention

Serious events: 0 serious events

Other events: 0 other events

Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Liliana Lengua, Ph.D.

University of Washington

Phone: 206-543-5655

Email: [email protected]

Results disclosure agreements

Principal investigator is a sponsor employee
Publication restrictions are in place