CClinicalTrials.gg
CompletedNCT05139251Updated Jan 31, 2024

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

An interventional study of Recovering from Intimate partner violence through Strengths and Empowerment (RISE) and ePALS in Positive Parenting, sponsored by The University of Texas Health Science Center, Houston. Completed at 1 site in United States. Open to female participants. Per ClinicalTrials.gov, last updated 2024-01-31.

Sponsored by The University of Texas Health Science Center, Houston · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
13
Allocation
Not applicable
Sex
Female
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Study 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.

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Conditions studied

  • Positive Parenting

Keywords

  • Positive parenting
  • Women experiencing homelessness
  • Inter-personal violence
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In context

Lead sponsor

The University of Texas Health Science Center, Houston is the lead sponsor of 880 studies on the registry; 209 are open to participants now.

Of its 170 completed or terminated interventional studies of FDA-regulated products, 140 (82%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

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

Exclusion Criteria:

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

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
13 participants (actual)

Study arms

  • Experimental
    Recovering from Intimate partner violence through Strengths and Empowerment (RISE) +ePALS

    Other: Recovering from Intimate partner violence through Strengths and Empowerment (RISE) · Other: ePALS

Interventions

  • OtherRecovering 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

  • OtherePALS

    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.

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What researchers measure

Primary outcomes

  1. 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

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  2. 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

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  3. 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

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  4. 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.

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  5. 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.

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  6. 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

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  7. 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.

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  8. 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.

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  9. 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.

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

  10. 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)

    Time frame: Baseline, 1 month post intervention, 3 months post intervention

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Study locations

1 site
  • The University of Texas Health Science Center at Houston
    Houston, Texas 77030, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 31, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05139251
Lead sponsor
The University of Texas Health Science Center, Houston
Responsible party
Doncy Eapen (Assistant Professor, The University of Texas Health Science Center, Houston) — Principal investigator
First posted
Dec 1, 2021
Start date
Sep 7, 2022
Primary completion
Jun 20, 2023
Completion
Oct 19, 2023
Last update
Jan 31, 2024

Study contacts

Doncy Eapen, PhD, RN, FNP-BC
principal investigator · The University of Texas Health Science Center, Houston

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2024. You cannot join it, but the record below documents what was studied.

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