Trial · NCT07888725
Feasibility Pilot of Remote Mindfulness Training Across Multiple Sites (REFORM Pilot)
NCT07888725, Not applicable, Not yet recruiting, Institute for Human Development and Potential (IHDP), Singapore
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Feasibility Pilot of Remote Mindfulness Training Across Multiple Sites (REFORM Pilot). Trials, record NCT07888725. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07888725
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Feasibility Pilot of Remote Mindfulness Training Across Multiple Sites (REFORM Pilot)
- NCT number
- NCT07888725
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- Institute for Human Development and Potential (IHDP), Singapore
- Conditions
- Psychological Stress
- Interventions
- Formal-Heavy Audio-Guided Mindfulness Training, Balanced Audio-Guided Mindfulness Training, Informal-Heavy Audio-Guided Mindfulness Training, Analytical Active-Control Training
- First posted
- 2026-10-22
- Last updated
- 2026-10-23
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Intervention adherence | Throughout the approximately 1-month intervention period | Number of the 12 scheduled audio-guided sessions completed by each participant. Session completion and adherence will be summarized descriptively to assess feasibility of the one-month intervention schedule. No quantitative go/no-go threshold is prespecified. |
| Secondary | Feasibility of Camera HRV data acquisition and transfer | Sessions 1, 6, and 12, over approximately 1 month | Number and proportion of scheduled Camera HRV measurements at Sessions 1, 6, and 12 that are successfully completed, transferred to the designated study inbox, reconciled using the participant study code, archived, and classified as valid according to the application's prespecified validity classification. |
| Secondary | Participant-reported feasibility and experience | At Session 12, approximately 1 month after enrollment | Participant experience with the study procedures will be assessed using the optional three-item REFORM Pilot Feedback Survey. Item-level responses will be summarized descriptively. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as |
|---|---|
| Go/No-Go Task | Primary outcome |
Source ConductCognition
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07888725
GET https://conductscience.org/api/trials/v1/NCT07888725/registered