Veterans Nature Therapy (Vet Hike)
- Conditions
- Posttraumatic Stress Disorders
- Interventions
- Behavioral: Group urban hikesBehavioral: Group nature hikes
- Registration Number
- NCT03997344
- Lead Sponsor
- University of Washington
- Brief Summary
This pilot study evaluates the feasibility of conducting a study to evaluate the impact of nature exposure/hiking in groups on symptoms of posttraumatic stress disorder in Veterans. Participants will be randomized to one of two groups: 1) nature hikes and 2) urban hikes.
- Detailed Description
Objectives and hypothesis: Posttraumatic stress disorder (PTSD) is a tragically common problem among US Military Veterans. Current treatment options for PTSD are not uniformly effective and dropout rates are high. Treatment approaches that are evidence-based, effective, and acceptable to Veterans are needed. Nature therapy is a promising, low-cost intervention, yet there are few rigorous studies that have evaluated it as a therapeutic intervention in Veterans with PTSD.
The specific aims of this study are to lay the ground work for a full-scale study by assessing the feasibility and acceptability of: i) recruitment, screening, and data collection methods; and ii) the nature hiking and urban hiking control group interventions. The investigators hypothesize that the interventions will be feasible and the recruitment, screening, and data collection methods will be acceptable.
Key eligibility criteria for this two-arm pilot randomized controlled trial include being a Veterans with PTSD, physical fitness/ability sufficient to walk for at least 2 hours, and willingness to complete assessments. Eligible individuals will be randomized to one of two groups: 1) nature hiking group, 2) urban hiking group. The investigators will enroll up to 60 individuals, to randomize up to 15 participants per group. Note that the number enrolled and randomized are not expected to be the same since he investigators anticipate some individuals who enroll will be determined not to be eligible based on responses to the baseline questionnaire. Individuals randomized to groups 1 or 2 will be invited to participate in six hikes of 2-4 hours in duration, over approximately 12 weeks. Individuals will be asked to complete questionnaires at baseline and weekly for 12 weeks, and then again at 24 weeks. The primary outcomes for this study relate to feasibility and acceptability. The investigators will collect information on time to recruit the sample, retention and survey completion at each time point, and attendance at hikes. A secondary aim is to ascertain changes in PTSD symptoms (which will serve as the primary outcome of the full-scale trial), secondary outcomes (e.g., quality of life) and mediators of the intervention, including factors such as depression, perceived stress, affect, loneliness, anxiety, social connectedness, rumination, and nature connection.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 26
- U.S. Military Veteran;
- Active PTSD symptoms based on the PCL-5;
- No diagnosis of schizophrenia, bipolar disorder, or other psychotic disorders (based on self-report);
- Low risk of suicide (based on responses to the MINI Suicidal module);
- No inpatient admission in last 3 months (based on self-report);
- No current alcohol disorder/dependence (based on having a score<16 on the 10-item self-administered AUDIT questionnaire);
- No evidence of drug-related problems (based on having a score <3 on the DAST-10)
- Capable of safely participating in hikes as evidenced by no "yes's" on the Physical Activity Readiness Questionnaire (or approval of their primary care physician) and individual assertion that they can walk at least 2 hours at an easy to moderate effort with breaks;
- Willing to be randomized to one of two groups and complete all study procedures;
- Able to provide written informed consent to participate.
- Schizophrenia, bipolar disorder or other psychotic disorder
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Urban hikes Group urban hikes Group hikes in a urban setting (e.g., downtown area) Nature hiking Group nature hikes Group hikes in a natural setting (e.g., park, wilderness area)
- Primary Outcome Measures
Name Time Method Recruitment Baseline Percentage of individuals contacted who are randomized
Retention 12-week follow-up Percentage of participants that complete assessments
- Secondary Outcome Measures
Name Time Method Quality of life/well-being: Satisfaction with Life Scale Baseline and 6-, 12-, 24-week follow-ups Satisfaction with Life Scale; 5-items, range 5-35; summed; higher = greater life satisfaction
Perceived stress Baseline and 6-, 12-, 24-week follow-ups Perceived Stress Scale 4 (PSS-4); 4-items, range 0-16; summed; higher = greater stress
Rumination Baseline and 6-, 12-, 24-week follow-ups State rumination- Rumination Reflection Questionnaire 12-items, range 5-60; summed; higher = greater rumination
Social connectedness Baseline and 6-, 12-, 24-week follow-ups 4-item Social Connectedness Scale; 4-items, range 4-28; summed; higher = greater connection to group
Depression Baseline and 6-, 12-, 24-week follow-ups Personal Health Questionnaire Depression Scale (PHQ-8); 8-items, range 3-24; summed; higher = greater depression
PTSD symptoms Baseline and 6-, 12-, 24-week follow-ups Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5), 20 items, range 0-80; summed; higher = greater PTSD
Trial Locations
- Locations (1)
VA Puget Sound Health Care System
🇺🇸Seattle, Washington, United States