Substance Abuse and Trauma in Incarcerated Women

Sponsor
University of Tulsa (Other)
Overall Status
Completed
CT.gov ID
NCT01413984
Collaborator
(none)
95
1
2
16
5.9

Study Details

Study Description

Brief Summary

The proposed study will evaluate Covington's Helping Women Recover (HWR) plus Beyond Trauma (BT) curriculum with female offenders at Eddie Warrior Correctional Facility in Taft, Oklahoma. The purpose of the proposed study is to expand previous findings by including a comparison group of women that are not receiving treatment but are otherwise eligible, and by using outside evaluators to conduct the assessments. Furthermore, this study will extend the outcomes measured in previous evaluations by including measures of sleep disturbance, posttraumatic cognitions, and a more extensive assessment of trauma-related symptoms. The hypotheses for this study are listed below:

  1. Incarcerated women with substance use disorders and history of trauma enrolled in the integrated treatment program (HWR plus BT) will report significantly fewer symptoms on measures of posttraumatic stress and associated cognitions, substance use, depression, and related symptoms following treatment than those in the comparison group.

  2. Those in the treatment group will improve significantly more than those in the comparison group on the symptoms listed above.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Helping Women Recover/Beyond Trauma
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
95 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Substance Abuse and Trauma in Incarcerated Women: An Effectiveness Study
Study Start Date :
Nov 1, 2010
Actual Primary Completion Date :
Mar 1, 2012
Actual Study Completion Date :
Mar 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: cognitive behavioral group treatment

Helping Women Recover/Beyond Trauma integrated substance abuse and trauma treatment group. (Dr. Covington)

Behavioral: Helping Women Recover/Beyond Trauma
Four treatment rounds will be conducted, and a goal of 20 women (10 from each group) will be recruited to participate in each round. A new treatment group will start every four months. Sessions are approximately 2 hours each, 3-4 times per week over four months in a group format. This treatment program will focus on the integrated treatment of trauma and substance abuse in women. Versions of the curriculum exist both for community and corrections populations. In this intervention the corrections version will be used.

No Intervention: comparison group

a comparison group of incarcerated women will receive the pre and post assessments with no interventions.

Outcome Measures

Primary Outcome Measures

  1. PTSD checklist (change from baseline at one week post treatment) [one-week before treatment, one week post treatment]

    17 item post traumatic stress disorder symptoms checklist will be administered pre treatment and one week following 4 month treatment completion.

  2. Trauma Related Nightmare Survey (change from baseline at one week post treatment) [one week before treatment, one week post treatment]

    brief assessment of nightmare frequency and severity to be administered pre-treatment and one week following 4 month treatment completion.

  3. Posttraumatic Cognitions Inventory (change from baseline at one week post treatment) [one week before treatment, one week post treatment]

    36 item assesment of cognitions related to world, self and blame to be administered pre-treatment and one week following 4 month treatment completion.

  4. CES-D, NIMH (change from baseline at one week post treatment) [one week before treatment, one week post treatment]

    Center for Epidemiologic Studies Depression Scale (CES-D), NIMH is a 20 item depression inventory to be administered pre-treatment and one week following 4 month treatment completion.

  5. Drug-Taking Confidence Questionnaire (change from baseline at one week post treatment) [one week before treatment, one week post treatment]

    50 item assessment of alcohol and drugs self efficacy to be administered pre-treatment and one week following 4 month treatment completion.

  6. Trauma Symptoms Inventory (change from baseline at one week post treatment) [one week before treatment, one week post treatment]

    100 item trauma symptoms questionnaire to be administered pre-treatment and one week following 4 month treatment completion.

Secondary Outcome Measures

  1. Parenting Stress Index for Incarcerated Women (change from baseline at one week post treatment) [one week before treatment, one week post treatment]

    two scales from the PSI and selected parenting issues from incarcerated women to be administered pre-treatment and one week following 4 month treatment completion.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Incarcerated women at Eddie Warrior Correctional Center (EWCC) in Taft, Oklahoma

  • The following 6 criteria are then employed at EWCC for HWR/BT treatment eligibility:

  1. An Level of Service Inventory (LSI) score of 30 or greater

  2. An LSI protective score of 15 or less

  3. 1.5 years or less remaining in prison

  4. A Case Plan identifying substance abuse treatment need

  5. Ability to read and comprehend

  6. 18 years of age or older

Exclusion Criteria:
  • Under age 18

  • Not incarcerated

  • More than 1.5 years remaining in prison

  • LSI score less than 30 or a protective of more than 15

  • No identified substance abuse need

  • Inability to read and comprehend

Contacts and Locations

Locations

Site City State Country Postal Code
1 Eddie Warrior Correctional Facility Taft Oklahoma United States 74463

Sponsors and Collaborators

  • University of Tulsa

Investigators

  • Principal Investigator: Rachael Swopes, M.S., University of Tulsa

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rachael Swopes, Graduate Student, University of Tulsa
ClinicalTrials.gov Identifier:
NCT01413984
Other Study ID Numbers:
  • TU 11-18
First Posted:
Aug 10, 2011
Last Update Posted:
Mar 18, 2014
Last Verified:
Mar 1, 2014
Keywords provided by Rachael Swopes, Graduate Student, University of Tulsa
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 18, 2014