Skip to content

Mindfulness Training in Military Spouses

Promoting Wellbeing in Military Spouses With Training

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03308344
Enrollment
106
Registered
2017-10-12
Start date
2017-10-02
Completion date
2019-07-31
Last updated
2019-08-06

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

Conditions

Psychological Stress

Brief summary

This project aims to contextualize the delivery of mindfulness training for military spouses and evaluate its effectiveness on measures of executive functions and psychological well-being.

Detailed description

In addition to psychological and physical health challenges that military service members face, military deployment is known to have deleterious effects on the entire family unit. The January 2010 issue of the New England Journal of Medicine reported medical data from over 250,000 wives of deployed soldiers. These women suffered from clinically significant levels of anxiety, depression, sleep disturbances, and adjustment disorders. Thus, the psychological profile of military spouses sadly parallels that of the military servicemembers. Unfortunately, the effect of deployment on the psychological health in military spouses is largely unstudied, and very few resilience-building programs are available for military families. Prior research showed that mindfulness training (MT), as a resilience-building program in civilian and military servicemembers, can effectively protect against degradation in of executive functions (i.e., attention, working memory) and benefit psychological well-being over high-demand intervals. While research evidence mounts that MT is beneficial for service members, there is almost no research examining the impact of MT on military spouses' cognitive functioning and psychological well-being. The present study aims to investigate if MT may successfully benefit cognitive functioning and psychological well-being in military spouses.

Interventions

BEHAVIORALMindfulness training

The present MT program includes topics related to mindfulness, emotion regulation, and connection. It will be delivered in short, weekly sessions.

Sponsors

University of Miami
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Participants will be assigned into three groups: (i) a mindfulness training with spouse trainers (MT-ST, n = 60) that will receive the training from peers who underwent an extensive training practicum; (ii) a mindfulness training with mindfulness expert trainer group (MT-ME, n = 30) that will receive the training from a mindfulness expert trainer; and (ii) a wait-list control group (WLC, n = 30) that will be tested before and after a no-training interval and may receive MT at a later time after their second testing if they are interested.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* English-speaking * Being in a relationship or married to U.S. Army active-duty member or veteran.

Exclusion criteria

* A non-controlled severe medical disease that might interfere with the performance in the study. * Any other condition that the investigator might deem problematic for the inclusion of the volunteer in a training study of this nature.

Design outcomes

Primary

MeasureTime frameDescription
Change in Sustained Attention to Response Task (SART)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.SART is used to assess attentional performance and mind wandering. The task uses a continuous performance paradigm involving button presses to frequently presented non-targets (numbers 1, 2, 4, 5, 6, 7, 8, and 9) but requires the participants to withhold their motor response to the infrequent target (number 3). The subjective experience of mind wandering during SART is assessed through experience sampling probes randomly presented throughout the task.
Change in Working Memory task (WM)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.WMMW is used to assess working memory performance

Secondary

MeasureTime frameDescription
Change in Self-Compassion Scale (SCQ)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.SCQ assesses self-compassion.
Change in Anxiety Sensitivity Index (ASI)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.ASI assesses the construct of anxiety sensitivity.
Change in Center for Epidemiological Studies Depression Scale (CES-D)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.This 20-item scale measures the major components of depressive symptomatology in the general population (i.e., nonpsychiatric persons older than 18).
Change in Perseverative Thoughts Questionnaire (PTQ)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.PTQ assesses stress due to reoccurring thoughts
Change in Marital SatisfactionChange from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.Marital Satisfaction questionnaire assesses the level of marital satisfaction.
Change in Positive and Negative Affect Scale (PANAS)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.PANAS assesses positive and negative affect. It consists of a list of descriptors of positive (e.g., 'interested', 'enthusiastic') and negative (e.g., 'irritable', 'upset') affects. Items are rated on a 5-point scale (1 = very slightly or not at all, 5 = extremely), according to how participants feel. The Positive Affect scale reflects the extent to which a person feels enthusiastic, active, and alert; the Negative Affect scale reflects unpleasant mood states, such as anger, disgust, and fear.
Demographic QuestionsDemographic questions will only be asked at the pre-intervention baseline (testing 1).General demographic questions will be asked to gather information about the participants, i.e. gender, age, partner ranking, partner deployment status etc.
Change in Cognitive Failures Questionnaire (CFQ)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.CFQ assesses one's attention and awareness.
Feedback regarding the trainingFeedback questions will be asked only at the second testing session (testing 2), which is an average of 5 weeks from the baseline.If participants were part of any of the training groups, they will be asked to provide feedback of the training.
Feedback regarding the testingFeedback questions will be asked only at the second testing session (testing 2), which is an average of 5 weeks from the baseline.A 10-item questionnaire for participants to express their views and motivations about the tasks completed during the testing session.
General questions regarding life tendenciesChange from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.General questions regarding life tendencies in a variety of situations during the past two weeks.
Practice LogsParticipants will complete paper practice logs tracking their daily practice (i.e., minutes) from the beginning through the study completion, which is an average of 5 weeks after the beginning of the intervention.Practice logs will be used to keep track of participants' daily mindfulness practice.
Change in Perceived Stress Scale (PSS)Change from the pre-intervention baseline (testing 1) to post-intervention (testing 2), which is an average of 5 weeks from the baseline.PSS assesses the degree to which situations in one's life are viewed as stressful within the past month. Individual items assess feelings of stress, nervousness, irritation at life's hassles, and perceptions of one's own coping and control over a situation.

Countries

United States

Outcome results

None listed

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