Depression Clinical Trial
— SRTSOfficial title:
Stress Resilience Training System
The Stress Resilience Training System (SRTS) program is a stress reduction and resilience
building system that blends cognitive training to anticipate the effects of stress with
advanced biofeedback to mitigate stress effects and aftereffects, using a game-based
learning framework on an iPad platform.
The proposed study will evaluate the effectiveness of the SRTS program at reducing perceived
stress, PTSD symptoms, depression, anxiety, sleep quality, coping, attrition and
class/operational performance among United States Navy service members.
Status | Completed |
Enrollment | 68 |
Est. completion date | May 2015 |
Est. primary completion date | May 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Subjects must be Sailors attached to the Training Support Center San Diego (USN). - All genders and ethnic groups are to be included in the study. Exclusion Criteria: - Subjects will be excluded from participation if they will not be at the command for a minimum of 4 months from the start date. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
United States Naval Medical Center, San Diego | Office of Naval Research (ONR), Perceptronics Solutions |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Compliance | • For both the SRTS and PMR iPad-based programs, compliance data will be collected and stored on each iPad. Data will include the number of times the program was opened, the date for each session and for how long the program was open on each occasion. Data will be downloaded from iPads when iPads are turned in at the end of two months. • Participants will also be asked to complete a self-report form, indicating how often, on average, they used the program and practiced the techniques per week. | end of program (2 or 4 months) | No |
Primary | Perceived Stress Scale-10 | This is a 10-item scale designed to measure the degree to which a person perceives aspects of their life as uncontrollable, unpredictable and overwhelming. Participants are asked to indicate how often they have felt a certain way in the last month. The scale utilizes a 5-point likert format with responses ranging from never to very often. | baseline, 2 months, 4 months | No |
Primary | Pittsburgh Sleep Quality Index (PSQI) | The scale consists of seven different components of sleep quality that sum to an overall sleep quality score. A global score of 0-5 indicates good sleep quality while a global score greater than 5 indicates poor sleep quality. The global score as well as the sleep latency and habitual sleep efficiency scores will be used as continuous variables (Buysse, 1989). | baseline, 2 months, 4 months | No |
Primary | Generalized Anxiety Disorder Measure (GAD-7) | The scale was initially developed to screen for generalized anxiety disorder, but has sensitivity and specificity to panic, social anxiety, and PTSD. The instructions ask respondents to indicate how often they have been bothered by problems over the past two weeks. Scores are obtained from likert responses that range from 0 "Not at all" to 4 "Nearly every day". The total score can range from 0 to 21, with scores of 5, 10, and 15 being cutpoints for mild, moderate, and severe anxiety, respectively. The measure will be utilized to gain anxiety symptom severity scores (Spitzer et al., 2006). | baseline, 2 months, 4 months | No |
Secondary | PTSD Checklist -Civilian Version (PCL-C) | The PCL is a 17-item self-report measure of the 17 DSM-IV symptoms of PTSD. The PCL has a variety of purposes, including screening individuals for PTSD, diagnosing PTSD and monitoring symptom change during and after treatment. We will use the PCL-C (civilian) version for this study. The PCL-C (civilian) asks about symptoms in relation to "stressful experiences." The PCL-C is useful because it can be used with any population. The symptoms endorsed may not be specific to just one event, which can be helpful when assessing survivors who have symptoms due to multiple events. Typically, it is optimal to assess traumatic event exposure to ensure that a respondent has experienced at least one Criterion A event. | baseline, 2 months, 4 months | No |
Secondary | Patient Health Questionnaire (PHQ-9) | The scale measures the severity of depressive symptoms an individual endorses; the range of scores is 0 to 27, with scores of 5, 10, 15, and 20 indicating mild, moderate, moderately severe and severe depression, respectively. The criteria for major depressive disorder (MDD) can be met when a respondent checks "nearly every day" on the first item and checks four of the following items at equal or greater than "more than half the days." The ninth item reflects one's degree of suicidal ideation (SI). We will have a licensed independent practitioner available to whom those with any SI endorsed will be referred for a risk assessment. The PHQ-9 score will be used as a continuous dependent variable (Kroenke et al., 2001). | baseline, 2 months, 4 months | Yes |
Secondary | Response to Stressful Experiences Scale (RSES) | The RSES is a 22-item assessment designed to measure how individuals respond to stress, adversity and trauma. It includes six factors: positive appraisal, spirituality, active coping, self-efficacy, learning and meaning-making and acceptance of limits. Responses for individual questions will be reviewed in addition to the overall score which reflects the strength of the trait (Johnson, 2008). | baseline, 2 months, 4 months | No |
Secondary | Brief COPE | The Brief COPE is a 28-item scale designed to measure how people cope with stressful situations. Factor analysis revealed 10 distinct subscales: self-distraction, active coping, denial, substance use, use of emotional support, use of instrumental support, behavioral disengagement, venting, positive reframing, and planning (Carver, 1997). | baseline, 2 months, 4 months | No |
Secondary | Unit Support | The scale measures an individual's perceived degree of cohesion and quality of relationships with other military personnel during a given period of time spent together. Respondents are asked to describe how much they agree or disagree to a number of statements. Scores are obtained on a 5 point likert scale with responses ranging from 1 Strongly disagree to 5 Strongly agree. Higher scores reflect a better quality of relationships and a more unified group (King et al., 2003). | baseline, 2 months, 4 months | No |
Secondary | Quality of Life Scale (QOLS) | The QOLS is a 16 item scale assessing quality of life in areas such as physical health, social connections, recreation, etc. (Burckhardt 193). | baseline, 2 months, 4 months | No |
Secondary | Performance Indicator | Command-determined performance data will be collected from Training Support Center San Diego. | 4 months | No |
Secondary | Attrition Rate | This will be measured as the percentage of service members who drop out of each respective training program. This information will be collected from the command. | 4 months | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05777044 -
The Effect of Hatha Yoga on Mental Health
|
N/A | |
Recruiting |
NCT04680611 -
Severe Asthma, MepolizumaB and Affect: SAMBA Study
|
||
Recruiting |
NCT04977232 -
Adjunctive Game Intervention for Anhedonia in MDD Patients
|
N/A | |
Recruiting |
NCT04043052 -
Mobile Technologies and Post-stroke Depression
|
N/A | |
Completed |
NCT04512768 -
Treating Comorbid Insomnia in Transdiagnostic Internet-Delivered Cognitive Behaviour Therapy
|
N/A | |
Recruiting |
NCT03207828 -
Testing Interventions for Patients With Fibromyalgia and Depression
|
N/A | |
Completed |
NCT04617015 -
Defining and Treating Depression-related Asthma
|
Early Phase 1 | |
Recruiting |
NCT06011681 -
The Rapid Diagnosis of MCI and Depression in Patients Ages 60 and Over
|
||
Completed |
NCT04476446 -
An Expanded Access Protocol for Esketamine Treatment in Participants With Treatment Resistant Depression (TRD) Who do Not Have Other Treatment Alternatives
|
Phase 3 | |
Recruiting |
NCT02783430 -
Evaluation of the Initial Prescription of Ketamine and Milnacipran in Depression in Patients With a Progressive Disease
|
Phase 2/Phase 3 | |
Recruiting |
NCT05563805 -
Exploring Virtual Reality Adventure Training Exergaming
|
N/A | |
Completed |
NCT04598165 -
Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support
|
N/A | |
Completed |
NCT03457714 -
Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial
|
||
Recruiting |
NCT05956912 -
Implementing Group Metacognitive Therapy in Cardiac Rehabilitation Services (PATHWAY-Beacons)
|
||
Completed |
NCT05588622 -
Meru Health Program for Cancer Patients With Depression and Anxiety
|
N/A | |
Recruiting |
NCT05234476 -
Behavioral Activation Plus Savoring for University Students
|
N/A | |
Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
Enrolling by invitation |
NCT03276585 -
Night in Japan Home Sleep Monitoring Study
|
||
Completed |
NCT03167372 -
Pilot Comparison of N-of-1 Trials of Light Therapy
|
N/A | |
Terminated |
NCT03275571 -
HIV, Computerized Depression Therapy & Cognition
|
N/A |