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Facilitating Psychological Closure and Emotional Change Through Mindfulness Meditation

Mindful Recollection: Attending to the Present Before Resolving the Past

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07437092
Enrollment
220
Registered
2026-02-27
Start date
2026-03-01
Completion date
2027-08-01
Last updated
2026-03-02

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

Conditions

Psychological Closure, Unresolved Event Memories

Keywords

Unresolved memories, Psychological closure, Closure, Mindfulness meditation

Brief summary

The goal of this clinical trial is to learn if mindfulness meditation can improve closure and emotion towards unresolved memories in an undergraduate student population. This will be tested through a brief, novel intervention called Mindful Recollection, where participants transition immediately from mindfulness meditation into the recollection of an unresolved memory. The secondary aim of the study is to investigate the mechanisms of change underlying Mindful Recollection. Overall then, the main questions this study aims to answer are: * Does mindful recollection reduce negative emotions associated with unresolved event memories? * Can increases in acceptance, decentering, and reappraisal account for the observed effects of mindful recollection on negative emotion? * Does mindful recollection facilitate closure towards unresolved event memories? * Can increases in acceptance, decentering, and reappraisal account for the observed effects of mindful recollection on closure? Researchers will compare the Mindful Recollection intervention to a mind-wandering control task to see if mindfulness meditation uniquely produces positive changes in emotion and closure above and beyond placebo. Mindful Recollection will involve a 13-minute audio-guided mindfulness meditation followed immediately by 2 minutes of memory recollection. The control task will involve 13-minutes of audio-guided mind-wandering followed immediately by 2 minutes of memory recollection. Participants will: * Complete pretest measures of emotion and closure towards an unresolved event memory. * Engage in either the Mindful Recollection intervention or the placebo control task after a 24-72 hour delay. * Complete post-test measures of emotion and closure towards the same unresolved event memory.

Interventions

BEHAVIORALMindfulness Meditation

Mindful Recollection consists of a 15-minute audio-guided task (13 minutes of guided meditation followed immediately by 2 minutes of unresolved event recollection). The 13-minute guided meditation is intended to facilitate a broad mindful awareness by working through sensations of the breath, body, and mind (in that respective order), eventually coming together in a practice of open monitoring - the non-selective observation of any and all aspects of experience. The 2-minute recollection period will have participants transition from meditating to recalling and reflecting on an unresolved memory they identified during the pretest period (approximately 24-72 hours prior).

BEHAVIORALMind-Wandering Task

The mind-wandering control task consists of a 15-minute audio-guided task (13 minutes of mind-wandering followed immediately by 2 minutes of unresolved event recollection). Mind-wandering is a common sham mindfulness technique that repeatedly prompts participants to let their thoughts flow freely, thinking about whatever comes to mind. This exposes participants to the same procedure (i.e., listening to a 13-minute audio-recording) without receiving guided mindful meditation instructions. Thus, this condition will guide participants to have a typical mental experience of thinking freely about whatever comes to mind, without developing a mindful awareness of their internal experience.

Sponsors

University of Windsor
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Ability to hear and understand spoken instructions clearly; English language proficiency

Exclusion criteria

* Trauma history/Dissociative tendencies

Design outcomes

Primary

MeasureTime frameDescription
Pre- to Post-Test Changes in Psychological Closure using the Closure and Resolution Scale (CRS)Baseline (24-72 hours prior to the intervention) and post-test (immediately after intervention)Items are rated on a 7-point Likert scale (1 = Completely disagree, 7 = Completely agree), with higher scores reflecting greater levels of closure and resolution.
Pre- to Post-Test Changes in Negative Emotion using the Positive and Negative Affect Schedule (PANAS)Baseline (24-72 hours prior to the intervention) and post-test (immediately after intervention)Items are rated on a 5-point Likert scale (1 = Not at all, 5 = Extremely), with higher scores reflecting a stronger endorsement of that emotional experience.

Secondary

MeasureTime frameDescription
Experiential Acceptance Towards Thoughts and EmotionsImmediately after the intervention (post-test)Using the acceptance subscale of The Southampton Experiential Avoidance and Acceptance Scale. Items are rated on a 7-point Likert scale (1 = Strongly disagree, 7 = Strongly agree), with higher scores indicating greater levels of openness towards internal experience.
ReappraisalImmediately after the intervention (post-test)Using the Regulation of Emotion Systems Survey. Items are rated on a 5-point Likert scale (1 = Strongly disagree, 5 = Strongly agree), with higher scores indicating greater engagement in reappraisal during the assigned task.
State DecenteringImmediately after the intervention (post-test)Using the Metacognitive Processes of Decentering-state scale. Items are rated on an 11-point Likert scale (0 = Not at all, 10 = Very much), with higher scores reflecting greater levels of state decentering (i.e., being aware of, disidentified with, and nonreactive to thoughts and emotions).

Countries

Canada

Contacts

CONTACTAnas Alsayed Hasan
alsayed4@uwindsor.ca647-224-1595

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026