Physiology of Liberation
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Boston University Charles River Campus
- Study ID
- NCT07780266
- Status
- Not Yet Recruiting
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Conditions
- Psychophysiological Reactivity and Recovery
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Brief Standardized Mindfulness/Attention Instruction — BEHAVIORALAt one or more assigned study measurement sessions, participants receive a brief, standardized, non-clinical instruction lasting approximately 1 to 10 minutes. The instruction directs attention to breathing or another clear body sensation, briefly acknowledges thoughts, emotions, wanting, resisting, or urges, and returns attention to the selected sensation. The number, duration, and schedule of sessions are specified before each study wave begins and applied consistently within that wave; comparison sessions are time-matched. Participants may open their eyes, change position, or stop at any time.
Study Details
This academic study examines how everyday experiences are related to short-term physiological reactivity and recovery and whether one or more brief standardized mindfulness/attention-instruction sessions change these patterns. Adults living in the United States who can read and understand the English study materials participate for up to 12 weeks and complete brief smartphone surveys several times a day during waking hours. Surveys include current experiences and recent alcohol and nicotine use; these reports are analyzed as contextual variables and are not automatic exclusion criteria. Some participants also use assigned non-invasive wearable sensors or blood-pressure monitors during prespecified measurement windows. Device output is used only for research measurement, not diagnosis, treatment, real-time medical decision-making, or patient management. In study waves with a randomized comparison, participants are randomized after consent to one or more brief mindfulness/attention-instruction sessions or time-matched no-instruction comparison sessions. Session duration, schedule, and allocation probabilities are specified before each study wave begins and applied consistently within that wave.
Key Dates
- First listed
- Aug 21, 2026
- Start date
- Sep 30, 2026
- Status verified
- Aug 2026
- Primary completion
- Aug 31, 2027
- Completion
- Sep 30, 2028
Study Design
- Enrollment
- 36 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Fixed Schedule - Instruction ThroughoutParticipants receive one or more brief standardized mindfulness/attention-instruction sessions at assigned measurement sessions and complete the same measurement schedule as the comparison arm. Each session lasts approximately 1 to 10 minutes. The number, duration, and schedule of sessions are specified before each study wave begins and applied consistently within that wave.
- No Intervention: Fixed Schedule - No InstructionParticipants sit quietly in a comfortable position as they normally would during one or more time-matched no-instruction comparison sessions. No particular attention or meditation method is requested. Each session lasts approximately 1 to 10 minutes. The number, duration, and schedule of sessions are specified before each study wave begins and applied consistently within that wave; participants complete the same measurement schedule as the experimental arm.
- Experimental: Within-Person Randomized InstructionBrief standardized mindfulness/attention instructions are delivered on randomly assigned day-blocks and withheld on the remaining day-blocks, with the sequence randomized within each participant and balanced across days of the week. All ecological momentary assessment and ambulatory physiological monitoring procedures are identical on instructed and non-instructed day-blocks. Each instruction session lasts approximately 1 to 10 minutes. Participation in any individual instruction is voluntary; whether the participant performed it is recorded.
Primary Outcome Measure
Time to 50% Return to Pre-Event Baseline Skin Conductance Level [ Time Frame: Repeatedly during each enrollment period of up to 12 weeks ]
Central Contacts
- Jiayin Sun, PhD617-353-9640
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Boston University Questrom School of Business | Boston | Massachusetts | 02215 |