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StressFeelSyncNCT06986850

FeelSync: Tailoring Ecological Momentary Assessments and Interventions for Emotion Awareness, Regulation, and Mental Health Outcomes

A study testing FeelSync mobile application and Ecological Momentary Assessment mobile application in people with Stress, run by Marta Marciniak at 1 site in Netherlands.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study investigates how different ways of reflecting on emotions in daily life influence emotional awareness, emotion regulation, and mental health. Using the FeelSync mobile app over the course of seven days, participants are prompted multiple times a day to report on their current emotional state in various… Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Stress
What is being tested?
FeelSync mobile application and Ecological Momentary Assessment mobile application
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
490 participants
Where
1 siteNetherlands
Study dates
12 Mar 2025to 31 Aug 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Owning a smartphone
  • Proficiency in English language
  • Being a student
  • Age between 18 to 30 years old

Who cannot join

  • Severe mental health disorder

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Marta A Marciniak, Dr contact

+31 10 754 5276

marciniak@essb.eur.nl

Netherlands1 site, 1 recruiting
  • Erasmus University Rotterdam

    Rotterdam

    Marta A Marciniak, Dr, +31 10 754 5276, marciniak@essb.eur.nl

    Recruiting

Other trials in Netherlands

About this study

This study investigates how different ways of reflecting on emotions in daily life influence emotional awareness, emotion regulation, and mental health. Using the FeelSync mobile app over the course of seven days, participants are prompted multiple times a day to report on their current emotional state in various formats (e.g., rating scales, multiple choice, or free text). In some groups, participants also receive brief daily exercises designed to help them practice cognitive reappraisal-a strategy that involves reframing stressful situations to reduce their emotional impact. The study aims to assess not only the overall effectiveness of these reappraisal exercises but also whether the type of emotional self-report used before the intervention affects its impact. All participants complete questionnaires before and after the app phase to track changes in mood, stress, emotional awareness, and regulation.

Conditions
Stress
Being tested
FeelSync mobile application, Ecological Momentary Assessment mobile application
Keywords
ecological momentary assessment, ecological momentary intervention, language, cognitive reappraisal, emotion regulation, emotion awareness, mental health
Medical subject headings
Language, Emotional Regulation, Psychological Well-Being

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • FeelSync mobile applicationDevice

    Ecological Momentary Intervention focused on cognitive reappraisal for distressing autobiographical memories, with a possibility to choose between distancing and positive reappraisal.

  • Ecological Momentary Assessment mobile applicationDevice

    Ecological Momentary Assessment used for self-monitoring of emotional states.

Study groups in NCT06986850
Study groupRoleWhat they receive
Ecological Momentary Assessment with self-generated emotion descriptionActive comparatorEcological Momentary Assessment with participant's self-generated emotion description in an open-ended question form, in English, provided five times daily for seven consecutive days
Receives: Device: Ecological Momentary Assessment mobile application
Ecological Momentary Assessment with pre-defined set of emotion items to selectActive comparatorEcological Momentary Assessment with pre-defined set of emotion items to select in a multiple-choice question form, in English, provided five times daily for seven consecutive days
Receives: Device: Ecological Momentary Assessment mobile application
Ecological Momentary Assessment with pre-defined set of emotion items to rate on a Likert scaleActive comparatorEcological Momentary Assessment with pre-defined set of emotion items to rate on a seven-point Likert scale, in a slider form, in English, provided five times daily for seven consecutive days
Receives: Device: Ecological Momentary Assessment mobile application
Ecological Momentary Intervention with self-generated emotion descriptionExperimentalEcological Momentary Intervention focused on cognitive reappraisal, with a possibility to choose between distancing and positive reappraisal, provided three times daily and preceded by Ecological Momentary Assessment with participant's self-generated emotion description in an open-ended question form, in English, provided five times daily for seven consecutive days
Receives: Device: FeelSync mobile application
Ecological Momentary Intervention with self-generated emotion description in mother tongueExperimentalEcological Momentary Intervention focused on cognitive reappraisal, with a possibility to choose between distancing and positive reappraisal, provided three times daily and preceded by Ecological Momentary Assessment with participant's self-generated emotion description in an open-ended question form, in participant's mother tongue, provided five times daily for seven consecutive days
Receives: Device: FeelSync mobile application
Ecological Momentary Intervention with pre-defined set of emotion items to selectExperimentalEcological Momentary Intervention focused on cognitive reappraisal, with a possibility to choose between distancing and positive reappraisal, provided three times daily and preceded by Ecological Momentary Assessment with pre-defined set of emotion items to rate on a seven-point Likert scale, in a slider form, in English, provided five times daily for seven consecutive days
Receives: Device: FeelSync mobile application
Ecological Momentary Intervention with pre-defined set of emotion items to rate on a Likert scaleExperimentalEcological Momentary Intervention focused on cognitive reappraisal, with a possibility to choose between distancing and positive reappraisal, provided three times daily and preceded by Ecological Momentary Assessment with pre-defined set of emotion items to rate on a seven-point Likert scale, in a slider form, in English, provided five times daily for seven consecutive days
Receives: Device: FeelSync mobile application

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Perceived Stress Scale

    Self-report questionnaire, Range: 0 - 40 Higher scores: Worse outcome (higher perceived stress)

    Measured: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)

  2. Beck Depression Inventory II

    Self-report questionnaire, Range: 0 - 63 Higher scores: Worse outcome (more severe depressive symptoms)

    Measured: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)

  3. State-Trait Anxiety Inventory

    Self-report questionnaire, [state scale only], Range: 20 - 80 Higher scores: Worse outcome (greater state anxiety)

    Measured: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)

  4. Emotion Regulation Questionnaire

    Self-report questionnaire, Reappraisal subscale: Range 1 - 7 (mean of 6 items) Higher scores: Better outcome (more frequent use of cognitive reappraisal) Suppression subscale: Range 1 - 7 (mean of 4 items) Higher scores: Worse outcome (more frequent use of suppression)

    Measured: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)

  5. Cognitive Emotion Regulation Questionnaire

    Self-report questionnaire, Subscale range: 2 - 10 per strategy

    Higher scores:

    On adaptive strategies (e.g., positive reappraisal, putting into perspective): Better outcome On maladaptive strategies (e.g., rumination, catastrophizing): Worse outcome

    Measured: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)

  6. Toronto Alexithymia Scale

    Self-report questionnaire, Range: 20 - 100 Higher scores: Worse outcome (greater difficulties in identifying and describing feelings; lower emotional awareness)

    Measured: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)

Secondary outcomes (1)
  1. Mobile Agnew Relationship Measure

    Self-report questionnaire, Range: 16-112 Higher scores: Better outcome (stronger perceived therapeutic alliance with the app/intervention)

    Measured: Follow-up (post intervention, study day 9)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 May 2025
  2. Study start12 Mar 2025
  3. Primary completion31 Aug 2025 (estimated)
  4. Study completion31 Aug 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Factorial
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
490 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06986850
Sponsor's protocol ID
ETH2425-0653
Acronym
FeelSync
Status last verified
May 2025
First submitted
15 May 2025
Last updated
23 May 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Only anonymized data from the self-report questionnaires will be shared via Open Science Framework.

Questions about this trial

What is this clinical trial studying?

A study testing FeelSync mobile application and Ecological Momentary Assessment mobile application in people with Stress, run by Marta Marciniak at 1 site in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 23 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Marta A Marciniak, Dr (+31 10 754 5276, marciniak@essb.eur.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Perceived Stress Scale (time frame: Baseline (pre-intervention, study day 1) and Follow-up (post intervention, study day 9)). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 May 2025; AzTrials last refreshed its copy on 31 Oct 2026.

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