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MOVE!+UP: Testing a Tailored Weight Management Program for Veterans With PTSD

MOVE!+UP: Testing a Tailored Weight Management Program for Veterans With PTSD

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04563741
Enrollment
174
Registered
2020-09-24
Start date
2020-10-01
Completion date
2025-03-26
Last updated
2026-05-06

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

Conditions

Obesity, Overweight, PTSD

Brief summary

Posttraumatic Stress Disorder (PTSD) is common among Veterans and results in poor psychological functioning, quality of life, and physical health. This includes having disproportionately high rates of obesity, in part due to PTSD symptoms interfering with physical activity and healthy diet. Unfortunately, Veterans with PTSD have poorer weight loss outcomes than those without PTSD in VA's existing weight management program, MOVE!. Based on pilot work, it appears that a weight management program that augments standard PTSD care and targets PTSD-related barriers to weight loss improves weight and PTSD symptoms. Whether it improves these issues more than standard VA care is in need of study, which is the focus of the proposed research. The proposed study also seeks to understand factors that would interfere with and facilitate implementing the program in VA if it is effective. This Veteran-centered, tailored weight loss program may efficiently benefit both physical and mental health of Veterans with PTSD, addressing standard care limitations.

Detailed description

Background: Post-traumatic stress disorder (PTSD), prevalent among Veterans, puts Veterans at increased risk for obesity and related conditions. Veterans with PTSD lose less weight in VA's MOVE! weight management program, due to PTSD symptoms that interfere with activity and healthy diet. In addition, many Veterans who receive evidence-based PTSD treatment remain symptomatic. A behavioral weight loss program that augments standard PTSD care and targets PTSD-related weight loss barriers called MOVE!+UP was piloted and iteratively refined among 44 overweight Veterans with PTSD. The fully developed MOVE!+UP is led by a psychologist and a Veteran peer support counselor, who provide complementary expertise. It includes 16 group sessions with 90 minutes of general weight loss support, coupled with Cognitive Behavior Therapy skills to address PTSD-specific barriers. Each session also includes a 30-minute community walk to address hypervigilance-based activity barriers and enhance classroom-based learning. Veterans receive two individual dietician visits, and counseling calls as needed. The cohort receiving the final MOVE!+UP package reported high satisfaction and had better weight loss outcomes than Veterans with PTSD in the general MOVE! program. They also reported substantial PTSD symptom reduction. Treatment targets like eating behaviors, activity, and insomnia also improved. MOVE!+UP effectiveness must be tested in a randomized trial. Significance/Impact: MOVE!+UP is timely and efficient, simultaneously addressing physical and mental health of a priority Veteran group. MOVE!+UP is positioned to address HSR&D priorities by promoting mental health and improving PTSD symptoms, access to care, and whole health. This study is aligned with HSR&D and ORD methodological priorities by using a hybrid type 1 trial. This study's cost and utilization analyses, and systematic identification of implementation barriers and facilitators, would place effectiveness findings in context and facilitate rapid translation to the field if MOVE!+UP is effective. This study will also provide insights about ways that general MOVE! and PTSD care can be enhanced to improve reach and effectiveness. Innovation: MOVE!+UP is the first weight loss program designed to address obesity in Veterans with PTSD. Specific Aims: This study proposes to enroll Veterans with PTSD who are classified as overweight or with obesity and who are engaged in PTSD care. They will be randomized to usual care enhanced with MOVE! (control) or usual care enhanced with MOVE!+UP (intervention), and is guided by three aims: 1) Test whether intervention participants have greater 6-month weight loss (primary outcome), and 6- and 12-month PTSD symptom reduction and 12-month weight loss (secondary exploratory outcomes), relative to controls; 2) Assess whether compared to control, intervention participants have greater improvements on 6-month treatment targets: physical activity, eating behavior, insomnia, depression, and social support; 3) Estimate intervention and control condition costs and utilization, and identify MOVE!+UP implementation barriers and facilitators, to contextualize Aim 1 and inform future implementation. Methodology: Hybrid type 1 trial with 164 Veterans with PTSD who are classified as overweight or with obesity and are currently enrolled in PTSD care. Implementation/Next Steps: This hybrid type 1 trial will provide data needed to prepare a MOVE!+UP implementation package for broader VA implementation if MOVE!+UP is effective. If it is not effective, Aims 2 and 3 will help understand how overweight Veterans with PTSD could be better supported in the future. Implementation activities would be coordinated with existing local, VISN, and national operational partners.

Interventions

BEHAVIORALMOVE!+UP

behavioral weight management intervention developed for Veterans with PTSD

BEHAVIORALMOVE!

standard VA weight management intervention

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcomes assessors will not know the treatment assignment. Because this is a behavioral intervention, with supervision provided by the lead investigator, the participants, care providers, and investigators will not be blinded.

Intervention model description

This is a hybrid type 1 trial with Veterans with PTSD who are classified as overweight or with obesity, and who are currently enrolled in PTSD care. Participants will be randomized to usual care enhanced with MOVE! (control) or usual care enhanced with MOVE!+UP (intervention).

Eligibility

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

Inclusion criteria

* PTSD Diagnosis: standard criteria for PTSD Checklist for DSM-5 (PCL-5): lifetime experience of trauma and a score of 33 * Overweight or obesity based on Body Mass Index (BMI) of 25 kg/m2 * Primary Care Provider or other physician approval * Willing to participate in all intervention or control and assessment activities * Enrolled in PTSD treatment * Must have active VA Puget Sound Health Care System medical record.

Exclusion criteria

* Not fluent in English, severe hearing loss, no phone access * Current MOVE! participation * Current pregnancy * Based on clinical judgment, would be unable to participate because of: * acutely exacerbated substance use, mental health, or chronic medical conditions * or moderate to severe chronic, progressive neurologic conditions such as Dementia * had bariatric surgery within the last 12 months or plan to undergo bariatric surgery within the next 6 months. * Report they cannot safely weigh themselves using the mailed study scale due to mobility issues or use of assistive devices * Baseline weight \>440 lbs

Design outcomes

Primary

MeasureTime frameDescription
Weight (Pounds) Change From Baseline to 6 Months Post-baselinebaseline and 6 months post-baselineThis study's primary aims is to test whether intervention participants have greater 6-month weight loss, relative to controls.

Secondary

MeasureTime frameDescription
Weight (Pounds) Change From Baseline to 12 Months Post-baselinebaseline and 12 months post-baselineTest whether intervention participants have greater long-term (12-month) weight loss, relative to controls.
PTSD Symptom Severity on the PTSD Checklist for DSM-5 Change From Baseline to 6 Months Post-baselinebaseline and 6 months post-baselineAssess whether compared to control, intervention participants have greater improvements on 6-month PTSD symptom severity. Total scores range 0 - 80, where higher scores are indicative of greater severity.
PTSD Symptom Severity on the PTSD Checklist for DSM-5 Change From Baseline to 12 Months Post-baselinebaseline and 12 months post-baselineAssess whether compared to control, intervention participants have greater improvements on 12-month PTSD symptom severity. Total scores range 0 - 80, where higher scores are indicative of greater severity.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKatherine D Hoerster, PhD MPH BA

VA Puget Sound Health Care System Seattle Division, Seattle, WA

Participant flow

Recruitment details

From 10/1/2020-2/28/2024, we sent recruitment materials to cohorts of randomly selected veterans meeting several VHA electronic health record (EHR)-based criteria. Potentially eligible patients were also identified from self or clinician referral. We then used manual chart review to determine whether patients met additional criteria. We then further phone-screened participants for self-reported eligibility. To determine final eligibility, study staff conducted a video visit to assess weight/BMI.

Pre-assignment details

We randomized 174 enrolled participants to MOVE! (control) or MOVE!+UP (intervention) in a 1:1 ratio within each recruitment cohort, using a permuted block design, with varying block sizes (2 or 4). People doing data collection and analysis remained masked until after 12-month data collection.

Baseline characteristics

Characteristic
Age, Continuous55 years
STANDARD_DEVIATION 13
Body Mass Index33.9 kg/m^2
STANDARD_DEVIATION 5.2
Household annual family income
> $100,000
22 Participants
Household annual family income
$40,001-60,000
20 Participants
Household annual family income
$60,001-$80,000
12 Participants
Household annual family income
$80,001-$100,000
16 Participants
Household annual family income
Less than or equal to $40,000
18 Participants
Household annual family income
Missing
3 Participants
Race/Ethnicity, Customized
Black or African-American
19 Participants
Race/Ethnicity, Customized
Hispanic or Latino--no
80 Participants
Race/Ethnicity, Customized
Hispanic or Latino--yes
9 Participants
Race/Ethnicity, Customized
Multiple categories
24 Participants
Race/Ethnicity, Customized
Other
7 Participants
Race/Ethnicity, Customized
White
107 Participants
Sex: Female, Male
Female
29 Participants
Sex: Female, Male
Male
57 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
2 / 890 / 85
other
Total, other adverse events
60 / 8960 / 85
serious
Total, serious adverse events
5 / 895 / 85

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026