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Passport to Freedom (P2F): Adaptation and Implementation of a Wellness Program

Passport to Freedom: Adaptation and Implementation of a Wellness Program to Educate and Empower Women Living in Transitional Housing Due to Intimate Partner Violence

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04069754
Enrollment
10
Registered
2019-08-28
Start date
2019-10-28
Completion date
2021-10-23
Last updated
2025-12-24

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

Conditions

Trauma

Keywords

trauma, stress, depression, coping, mindfulness

Brief summary

Women currently residing at an emergency shelter for women and children will participate in group sessions that cover topics that promote physical and emotional well-being through a combination of mindfulness exercises and health promotion activities..

Detailed description

In a group setting, the intervention will cover topics such as Mindfulness, Health (examine impact of trauma and stress on physical and mental well-being), Healthy relationships, Family matters (coping with conflicts) and Reflection session. Each group session (5) will last approximately 90 minutes, once weekly, and begin and end with mindfulness exercises. The women are also encouraged to download free mindfulness apps to practice the exercises between sessions. Women enrolled will receive health information that will cover a range of chronic health topics (pain, asthma, hypertension, diabetes, obesity), to complement already existing tools on mental health and post traumatic syndrome. Women enrolled will complete surveys: baseline questionnaires, a pre and post survey during each session, and follow-up questionnaires 4 weeks after the intervention.

Interventions

BEHAVIORALAdapted Passport to Freedom

5 weekly, 90 minute group sessions that cover topics such as mindfulness, health, healthy relationships, family matters, and reflections.

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

All participants will receive the intervention. There are no other groups.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years of age or older * Able to read and write English * Currently residing at the House of Ruth Maryland emergency shelter or onsite transitional housing.

Exclusion criteria

* Under 18 years of age * Inability to speak or write English * Physical or mental health conditions that would prevent meaningful group participation.

Design outcomes

Primary

MeasureTime frameDescription
Change in Physical Health as assessed by the Perceived Health Competence ScaleBaseline, 9 weeksThe Perceived Health Competence Scale measures the degree to which an individual feels capable of effectively managing their health. The score could range from 2-10. The higher the score, the greater the patient's perceived health competence.
Change in Mental Health as assessed by the Patient Health QuestionnaireBaseline, 9 weeksPatient Health Questionnaire assesses patient's level of distress and functional impairment. Score ranges from 0-4 depression severity is minimal or none. Score range from 5-9 is mild depression severity. Score range from 10-14 is moderate depression severity. 15-19 range is moderately severe depression. Range 20-27 indicates severe depression.

Secondary

MeasureTime frameDescription
Change in Stress as assessed by Everyday Stressor IndexBaseline, 9 weeksThe Everyday Stressor Index assesses the problems faced on a daily basis by low-income mothers with young children. The instrument has a possible range of 20-80. A higher score indicates a higher level of daily stress.
Change in Emotions as assessed by Difficulties in Emotion Regulation Scale-Short FormBaseline, 9 weeksThe Difficulties in Emotion Regulation Scale is a self report measure of subjective emotion ability. The measure yields a total score sum as well as scores on six sub-scales. All subscales are scored so that higher values reflect greater difficulty with emotion regulation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026