Ignite Creation Date:
2024-05-06 @ 6:01 PM
Last Modification Date:
2024-10-26 @ 2:40 PM
Study NCT ID:
NCT05516108
Status:
COMPLETED
Last Update Posted:
2024-06-12
First Post:
2022-08-18
Brief Title:
Remote Mindfulness Training Following Early Life Adversity
Sponsor:
University of Pittsburgh
Organization:
University of Pittsburgh
Study Overview
Official Title:
Smartphone-based Mindfulness Training for Health Following Early Life Adversity
Status:
COMPLETED
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
ReMind
Brief Summary:
This study will test the feasibility of delivering smartphone-based mindfulness and coping interventions to a sample of emergingyoung adults with a history of early life adversity ELA 80 participants with a history of ELA will be randomly assigned to complete a two-week mindfulness training intervention or matched coping control intervention both involving 14 foundational audio-guided lessons and practice prompts randomly delivered 3x daily At baseline post-intervention and one-month follow-up lab assessments participants will complete questionnaires and provide blood samples for assessment of markers of inflammation Data assessing subjective and physiological stress in daily life will be collected during the intervention and for one week before immediately after and one month after the intervention Passive sensor data will be continuously collected from participants smartphones and wearable devices to develop exploratory models that estimate and predict daily life stress Data will be used to evaluate feasibility and acceptability of interventions and assessments in an ELA sample test effects of mindfulness training on daily life stress and markers of inflammation in an ELA sample and develop exploratory machine learning models of stress from passive sensor data
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| K01AT011232 | NIH | None | httpsreporternihgovquickSearchK01AT011232 |