NCT00457522

Brief Summary

Although abuse by an intimate partner is very common and has serious negative effects on women's health, few studies have been done to test ways to increase safety for women in abusive relationships. This study will test a telephone intervention for women who report physical, emotional, and/or sexual abuse within the past 12 months, to see if

  • women use more safety behaviors and access more community resources
  • chronic pain, fatigue, depressive, and post-traumatic stress disorder (PTSD) symptoms affect a women's ability to use safety behaviors and access community resources.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2006

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2006

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2006

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 5, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

April 6, 2007

Completed
Last Updated

January 18, 2018

Status Verified

January 1, 2018

First QC Date

April 5, 2007

Last Update Submit

January 16, 2018

Conditions

Keywords

intimate partner violencedepressionPTSDfatigue

Outcome Measures

Primary Outcomes (2)

  • Number of safety promotion behaviors at initiation and completion of intervention

  • Number of community resources accessed at initiation and completion of intervention

Secondary Outcomes (2)

  • Stage of readiness for change at initiaion and completion of intervention

  • Severity of pain, fatigue, depressive and PTSD symptoms at initiation and completion of intervention

Interventions

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • female
  • years of age or older
  • speaks English
  • reports physical, emotional, and/or sexual abuse by an intimate partner within past 12 months

You may not qualify if:

  • non-English speaking
  • currently pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Shepherd's Clinic

Baltimore, Maryland, 21215, United States

Location

MeSH Terms

Conditions

DepressionStress Disorders, Post-TraumaticFatigue

Interventions

Nurses

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorStress Disorders, TraumaticTrauma and Stressor Related DisordersMental DisordersSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Health PersonnelHealth Care Facilities Workforce and Services

Study Officials

  • Anne B Woods, PhD, CNM

    Johns Hopkins University School of Nursing

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 5, 2007

First Posted

April 6, 2007

Study Start

April 1, 2006

Study Completion

December 1, 2006

Last Updated

January 18, 2018

Record last verified: 2018-01

Locations