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Feasibility of a Positive Parenting Program for Women Experiencing Homelessness Who Have a History of Interpersonal Violence

Feasibility of a Positive Parenting Program for Women Experiencing Homelessness Who Have a History of Interpersonal Violence: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06246773
Enrollment
28
Registered
2024-02-07
Start date
2024-03-26
Completion date
2025-10-24
Last updated
2026-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Homelessness, Interpersonal Violence

Keywords

Women experiencing homelessness (WEH), Positive Parenting

Brief 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 interpersonal violence (IPRV) and homelessness and to promote positive parenting strategies through Play and Learning Strategies (PALS), an evidence based intervention.

Interventions

During the first week, women will receive one session of Recovering from Intimate partner violence through Strengths and Empowerment (RISE) and from week 2 they will receive RISE and PALS simultaneously. Participants will receive four to six components of RISE - education on health effects of violence, improving coping and self-care, enhancing social support, and addressing sexual violence, increase safety planning, and assist in making difficult decisions. During each of the PALS sessions, parents will receive instruction on four responsive parenting constructs: contingent responsiveness, warm sensitivity (responses include high levels of affection and understanding of child states), maintaining vs. redirecting attention to objects and topics of conversation, and verbal scaffolding .In addition to direct instruction, parents will video-record themselves interacting with their child and engage in self-reflection of their own parenting behavior.

BEHAVIORALUsual Care

Participants will receive services available to them at the shelter or housing facility

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER
Rita and Alex Hillman Foundation - Hillman Emergent Innovation
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* report of at least one physically violent act from a partner within the past 24 months * have at least one child 5 years or younger.

Exclusion criteria

* do not speak English * their intimate partner is physically present at the time of enrollment

Design outcomes

Primary

MeasureTime frameDescription
Change in Women's parenting stress as assessed by the Parental Stress scale (PSS)Baseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionThis is an 18 item questionnaire and each is scored on a 5 point scale from 1(strongly disagree) to (5strongly agree) for a score range of 18-90, higher score indicating more stress
Change in social support as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Item Bank v 2.0 Emotional SupportBaseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionThe 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
Change in social support as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Item Bank v 2.0 Informational SupportBaseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionThe 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
Change in women's empowerment as assessed by the Personal Progress Scale-Revised (PPS-R)Baseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionPPS-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.
Change in self efficacy as assessed by the General Self- Efficacy Scale (GSE)Baseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionGSE 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.
Change in parent satisfaction as assessed by the Parenting Sense of Competence Scale (PSOC)Baseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionThe 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
Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-InfantBaseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionDECA (Infant) is a 33 item questionnaire for parents about their infants (1month-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.
Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-ToddlerBaseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionDECA (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.
Change in children's behavior as assessed by the Devereux Early Childhood Assessments (DECA)-PreschoolersBaseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionDECA (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
Change in perceived parent child connectedness as assessed by the Mothers Object Relational Scale- Short Form (MORS- SF) and MORS- Child scale.Baseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionThis measures mothers' perception on 2 scales: warmth and invasiveness. This is a 14 item scale and each item is scored from 0( never)-5(always).Warmth is scored by adding the scores from items 1,3,4,6,8,11,and 13, for an average score of 29 a higher score indicating more warmth. Invasiveness is scored by adding the scores of items 2,5,7,9,10.12.and 14, an average score of 10 and higher score indicates worse outcome.

Secondary

MeasureTime frameDescription
Change in usability assessed by the System Usability Scale (SUS)Baseline, immediately after intervention(about 6 weeks after baseline), One month after end of intervention and 3 months after end of intervention interventionThis is a 10-item questionnaire and each is scored from 5 (strongly agree) to 1 (strongly disagree), maximum score range is 0-100, higher number indicating better usability.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORDoncy J Eapen, PhD, MSN, APRN, FNP-BC

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026