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VA Home-Based Emotional Learning With Practical Skills

VA Home-Based Emotional Learning With Practical Skills (VA-HELPS): Treatment for Depressed and/or Anxious Rural Veterans in Home-Based Primary Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01685528
Acronym
VA-HELPS
Enrollment
18
Registered
2012-09-14
Start date
2012-12-31
Completion date
2015-12-31
Last updated
2016-04-07

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

Conditions

Anxiety, Depression

Keywords

Anxiety, Depression, Geriatric, Veteran

Brief summary

The purpose of this study is to determine the feasibility and acceptability of providing evidence-based, person-centered, culturally tailored treatment for anxiety and/or depression via telephone to rural Veterans receiving home-based primary care.

Detailed description

VA-HELPS will include flexibility in both content and delivery to meet the needs of Home Based Primary Care (HBPC) Veterans. Content will be modular to meet the needs of both anxious and depressed participants. Modular skills-based treatment has been used successfully with a range of clinical problems (Chorpita et al., 2004; Henin et al., 2001; Wetherell et al., 2009, 2011), including our own group's work treating generalized anxiety disorder (GAD) in primary care (Calleo et al., in press) and anxiety-depression in patients with chronic illness (Cully et al., 2010). To further support a patient-centered treatment approach, patients will have the opportunity to include R/S. Research points to the importance of R/S in coping with illness, with 50-90% of patients reporting using their belief systems to enhance coping skills (Koenig & Adams, 2008). Along with content modifications, delivery of treatment should complement the needs of HBPC Veterans. Providing one initial in-home session, followed by telephone contact for subsequent sessions, allows cost effectiveness to be taken into consideration; and greater numbers of rural HBPC patients will have access to the intervention. Treatment will involve approximately 6 to 8 weekly sessions lasting approximately 30-40 minutes each. After the first in-person session, all sessions will be delivered via telephone. At least one booster call (15-20 minutes) will occur during the month following completion of active treatment. All participants will complete assessments at baseline, 8 weeks, and 12 weeks.

Interventions

BEHAVIORALCBT

6-8 weekly sessions of CBT, 1 of which is in person with the rest being over the telephone

Sponsors

South Central VA Mental Illness Research, Education & Clinical Center
CollaboratorFED
Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 or older * Part of Home-Based Primary Care * Reside in a rural community, as defined by the US Census Bureau * Symptoms of anxiety and/or depression

Exclusion criteria

* Significant cognitive impairment * Active suicidal intent * Current uncontrolled psychosis, bipolar, or substance-abuse disorders within the past month

Design outcomes

Primary

MeasureTime frame
Geriatric Anxiety Inventory12 weeks
Penn State Worry Questionnaire (PSWQ-A)12 weeks
Generalized Anxiety Disorder-712 weeks

Secondary

MeasureTime frameDescription
Patient Health Questionnaire-912 weeks
Geriatric Depression Scale12 weeks
SF-12 Health Survey12 weeks
Brief Multidimensional Measure of Religiousness and Spirituality12 weeks
Insomnia Severity Index12 weeks
Working Alliance Inventory12 weeks
Brief RCOPE12 weeksA measure of positive and negative forms of religious coping
Client Satisfaction Questionnaire12 weeks

Countries

United States

Outcome results

None listed

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