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Family Involvement in Treatment for PTSD

24 mars 2015 uppdaterad av: US Department of Veterans Affairs

Perspectives on Enhancing Family Involvement in Treatment for PTSD

Post-traumatic stress disorder (PTSD), prevalent among returning OEF/OIF/OND Veterans, has a powerful impact on family functioning. Good family relationships appear to moderate its impact; stressful relationships may reduce the benefits of treatment. A program that assists both Veteran and family in coping with the Veteran's PTSD could directly improve the Veteran's re-adjustment and well-being and indirectly improve his/her social and occupational functioning.

Studieöversikt

Status

Avslutad

Detaljerad beskrivning

Background: Post-traumatic stress disorder (PTSD), a potentially severe and persistent condition that affects social, occupational and family functioning, is prevalent among returning OIF/OEF veterans. PTSD has a powerful impact on family functioning. Because good family relationships appear to moderate its impact, while stressful relationships may reduce the benefits of treatment, a program that enhances family functioning by assisting both veteran and family in coping with the veteran's PTSD could directly improve the veteran's adjustment and well-being, and indirectly improve his/her social and occupational functioning. Effective programs for OIF/OEF veterans are urgently needed. This study will address critical gaps in knowledge about relevant needs and preferences of OIF/OEF veterans and families, and how best to involve families in treatment.

Objectives: The specific aim of this project is to describe the needs and preferences of OIF/OEF service-era veterans with PTSD and their families relevant to family involvement in care.

Methods: This two-site study was conducted at the Central Arkansas Veterans Healthcare System (CAVHS, Little Rock, AR) and Oklahoma City (OKC) VAMCs. Qualitative (focus-group or individual) interviews were conducted with 47 Veterans (33 CAVHS, 14 OKC) and 36 Veteran-designated family members (19 CAVHS/17 OKC). Veterans were eligible if they were 18-65 years of age, had served in Iraq or Afghanistan since October 2001, had received treatment for PTSD at the CAVHS or OKC VAMCs in the previous 12 months, and had an adult family member who might be willing to participate in an interview. Family was defined broadly to include relatives, significant others, and friends the Veteran considered "as close as family." Interviews addressed perceived needs related to the Veteran's readjustment to civilian life, desires for family involvement in treatment, types of services that were/would have been helpful and attractive during readjustment, as well as logistic considerations (e.g., frequency of meetings). Qualitative data were analyzed using the techniques of constant comparison and content analysis. Demographic data, deployment data, and data on preferred program structure and format were collected via an anonymous paper-and-pencil questionnaire administered following the qualitative interview.

Status: Data collection and analysis of main themes are complete. In depth analysis of additional themes is ongoing.

Studietyp

Observationell

Inskrivning (Faktisk)

83

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Arkansas
      • No. Little Rock, Arkansas, Förenta staterna, 72114-1706
        • Central Arkansas Veterans Healthcare System Eugene J. Towbin Healthcare Center, Little Rock, AR
    • Oklahoma
      • Oklahoma City, Oklahoma, Förenta staterna, 73104
        • VA Medical Center, Oklahoma City

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Veteran participants were OIF/OEF veterans receiving outpatient treatment for PTSD at the Little Rock or Oklahoma City VAMCs. Each veteran participant was asked to designate an adult family member/friend to participate in a separate interview.

Beskrivning

Inclusion Criteria:

Veteran:

  1. Age 18-65;
  2. 2 or more inpatient or outpatient mental health contacts at LR or OKC VAMC in the previous 12 months with a primary diagnosis of PTSD;
  3. Served in Iraq or Afghanistan since 10/7/01;
  4. Have a family member who may be willing to participate in the focus group.

Family:

  1. Age > 18
  2. English speaking
  3. Be the designated "family member" of a participating veteran

Exclusion Criteria:

  • Non-English speaking

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Kohorter och interventioner

Grupp / Kohort
Group 1
Male veterans (focus groups and individual interviews)
Group 2
Female veterans (focus groups and individual interviews)
Group 3
Family members of participating veterans (focus groups and individual interviews)

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Qualitative Interviews - Perspectives on Family Involvement in PTSD Treatment
Tidsram: During the 1-1.5 hour interviews
This is qualitative research. "Outcomes" were themes raised with regard to content to be included in a multi-family group psychoeducation program for OEF/OIF/OND veterans with PTSD and family members.
During the 1-1.5 hour interviews

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Ellen P. Fischer, PhD, Central Arkansas Veterans Healthcare System (North Little Rock)

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 november 2009

Primärt slutförande (Faktisk)

1 oktober 2011

Avslutad studie (Faktisk)

1 mars 2012

Studieregistreringsdatum

Först inskickad

1 maj 2009

Först inskickad som uppfyllde QC-kriterierna

4 maj 2009

Första postat (Uppskatta)

5 maj 2009

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

14 april 2015

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

24 mars 2015

Senast verifierad

1 mars 2015

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • DHI 08-097
  • CAVHS 0156_2008I (Annan identifierare: CAVHS IRB)

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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