CompletedNot Applicable

Comparing the Effectiveness of Reappraisal Strategies in Adult Participants

Turkey (Türkiye)233 participantsStarted 2025-09-21

Plain-language summary

The goal of this clinical trial is to learn which reappraisal strategy works better to reduce sadness and anxiety in emerging adults. The main questions it aims to answer are: What is the effect of emotion regulation strategies (reconstrual, repurposing) on short term negative emotions (anxiety, sadness)? Does the effectiveness of these strategies vary depending on the type of emotion (anxiety vs. sadness)? Are reconstrual and repurposing more effective compared to active and passive control conditions? What is the effect of these strategies on short-term positive emotions (e.g., hope, happiness)? Researchers will compare reconstrual and repurposing strategies to see which one is more effective in improving emotional outcomes. Participants will: be randomly assigned to one of eight conditions in a 4 (Regulation Strategy: Reconstrual, Repurposing, Active Control, Passive Control) × 2 (Emotion Type: Sadness vs. Anxiety) factorial design. Complete online tasks and surveys about their emotions

Who can participate

Age range

18 Years – 30 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Aged 18-30 years * Fluent in Turkish * No current psychiatric treatment or diagnosis (self-reported) * Willingness to participate and provide informed consent Exclusion Criteria: * History of severe psychiatric or neurological disorders * Current substance use disorder

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change in Negative Affect

Timeframe: Immediately after vignette exposure vs. immediately after intervention

Change in valence and arousal

Timeframe: Immediately after vignette exposure vs. immediately after intervention

Trial details

NCT IDNCT07008209

SponsorIbn Haldun University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-01-05

View on ClinicalTrials.gov More Emotional Dysregulation trials