Positive Parenting: Empowering Young Mothers Experiencing Homelessness With a History of Inter-personal Violence to Improve Parenting Strategies

Positive Parenting Clinical Trial

Official title:

Positive Parenting: Empowering Young Mothers Experiencing Homelessness With a History of Inter-personal Violence to Improve Parenting Strategies

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05139251
• Other study ID #: HSC-SN-21-0869
• Status: Completed
• Phase: N/A
• Start date: September 7, 2022
• Est. completion date: October 19, 2023

Study information

• Verified date: January 2024
• Source: The University of Texas Health Science Center, Houston
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to strengthen the skills and self-efficacy of women by addressing the social and emotional trauma that they have experienced from inter-personal violence (IPRV) and homelessness and to promote positive parenting strategies through Play and Learning Strategies (ePALS), an evidence based intervention.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: October 19, 2023
• Est. primary completion date: June 20, 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• women's report of physical, sexual or psychological abuse from a partner/ family member/ acquaintance/ stranger within the last 24 months
• have at least one child under the age of 5 years old

Exclusion Criteria:

• non-English speaking
• physical presence of a male partner at the time of enrollment

Related Conditions & MeSH terms

• Positive Parenting

Intervention

Other:
• Recovering from Intimate partner violence through Strengths and Empowerment (RISE)
RISE intervention will be implemented for a period of 4 weeks at the beginning of the program. Four components/modules of the RISE intervention which includes a) education on health effects of violence, b) improving coping and self-care, c) enhancing social support, and d) addressing sexual violence will be used. Toward the beginning of each session the participant will complete a brief survey including a 10-item general self-efficacy scale to be graphed and discussed together to provide more immediate feedback to women about their progress, and at times, inform module selection. At the conclusion of each RISE session, women are asked to set a goal related to the topic in consultation with the clinician
• ePALS
Participants and their children will then receive 6 weekly sessions of ePALS. The ePALS sessions include rapport building, recognizing and understanding children's signals, contingently responding to signals, labeling objects and actions, learning book reading strategies, maintaining children's focus of attention, helping children with self-regulation, and language scaffolding techniques. Each parent will have a personal parenting coach who remotely supports their progress through the program. After a parent views a PALS coaching session, they will videotape themselves trying the strategy for that week with their child. Then their coach sets up a zoom call and together they talk about the PALS strategy and view the video. The coach facilitates parental appraisal of their behavior and discuss what they thought worked with their child and what they want to do differently.

Locations

Country	Name	City	State
United States	The University of Texas Health Science Center at Houston	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
The University of Texas Health Science Center, Houston

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Women's parenting stress as assessed by the Parental Stress scale (PSS)	PSS is an 18-item questionnaire and the participants rate each item on a scale ranging from 1 ("strongly disagree") to 5 ("strongly agree"), a higher score indicating more stress	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in social support as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Item Bank v 2.0 Emotional Support	The PROMIS emotional support tool has 16 items and the participants respond each item using a 5-point rating scale from 1(never)-5(always) a higher score indicating more emotional support	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in social support as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Item Bank v 2.0 Informational Support	The PROMIS informational support is a 10 items and participants respond each item using a 5-point rating scale (Health Measures) anchored by 1(never)-5(always) with a higher score indicating a better outcome	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in women's empowerment as assessed by the Personal Progress Scale-Revised (PPS-R)	PPS-R is a 28-item self-report measure on which participants rate the extent to which they agreed or disagreed with each item on a 7-point scale.	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in self efficacy as assessed by the General Self- Efficacy Scale (GSE)	GSE is a 10 item scale. Participants respond to statements such as "I can solve most problems if I invest the necessary effort" on a 4-point Likert scale anchored by 1(not at all true)-4( exactly true),the total score ranges between 10 and 40, with a higher score indicating more self-efficacy.	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in parent satisfaction as assessed by the Parenting Sense of Competence Scale (PSOC)	The PSOC is a 17-item scale and each item is rated on a 6-point Likert scale anchored by 1(strongly disagree to 6( strongly agree).A higher score indicates a higher parenting sense of competency	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-Infant	DECA (Infant) is a 33 item questionnaire for parents about their infants (1mont-18 months) It is a 5 point behavior rating scale scored from never to very frequently which provides an assessment of within-child protective factors central to social and emotional health and resilience.	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-Toddler	DECA (Toddler) is a 36 item questionnaire. It is a 5 point behavior rating scale scored from never to very frequently which provides an assessment of within-child protective factors central to social and emotional health and resilience.	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-Preschoolers	DECA (preschoolers) is a 38 item questionnaire. It is a 5 point behavior rating scale scored from never to very frequently which provides an assessment of within-child protective factors central to social and emotional health and resilience.	Baseline, 1 month post intervention, 3 months post intervention
Primary	Change in perceived parent child connectedness as assessed by the Mothers Object Relational Scale- Short Form (MORS- SF) and MORS- Child scale.	this is a 14 item scale and each item is scored from 0( never)-5(always)	Baseline, 1 month post intervention, 3 months post intervention