Skip to content
Clinical Trials – home
Not recruiting

Study of Escitalopram Effects on Learning and Decision-Making in Healthy Adults: A Comparison with Placebo

Verified siteRegistered drug
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

What is this trial about?

A plain-language summary of the goals, design and what participants do

This study aims to understand how serotonin affects learning and decision-making in healthy individuals. The research involves the use of escitalopram, a medication that influences serotonin levels in the brain, and a placebo. Escitalopram belongs to a group of medications commonly used to treat depression, though this study focuses on its effects in healthy people.

The study will examine how the medication affects participants' ability to make decisions and learn from their experiences. Participants will receive either escitalopram tablets or placebo capsules by mouth. The medication will be taken for a period of up to 24 weeks, with a maximum daily dose of 20 mg of escitalopram.

During the study, participants will complete various behavioral tasks and questionnaires to measure their decision-making abilities. The tasks will assess how quickly and accurately participants respond to different situations. The study uses a controlled approach where some participants receive the active medication while others receive the placebo, allowing researchers to compare the effects of escitalopram on learning and decision-making processes.

The research process

The trial runs in 3 steps – from screening to follow-up. Each step says what happens and what the team monitors.

  1. Step 1

    Initial assessment

    You will be confirmed as a healthy volunteer between 18-40 years of age

    If you can bear children, a pregnancy test will be conducted to confirm negative status

  2. Step 2

    Medication assignment

    You will receive either:

    Escitalopram 10 mg film-coated tablet for oral use

    Or

    A placebo capsule containing microcrystalline cellulose for oral use

  3. Step 3

    Behavioral tasks

    You will complete a resource investment task that measures accuracy and reaction times

    You will participate in 4 additional behavioral tasks measuring accuracy and reaction times

    You will respond to questionnaires about individual characteristics

Who can join the trial?

5 criteria

  • Must be a healthy volunteer (a person who does not have any significant medical conditions)
  • Age must be between 18 and 40 years old
  • Both men and women can participate
  • For participants who can become pregnant: must have a negative pregnancy test during the initial screening visit
  • Must not be part of any vulnerable population groups (such as people unable to give consent)

Who cannot join the trial?

15 criteria

  • History of neurological disorders (conditions affecting the brain, nerves, and spinal cord)
  • History of psychiatric disorders (mental health conditions)
  • Current use of medications that affect brain function or behavior
  • History of substance abuse or addiction
  • Pregnancy or breastfeeding
  • Inability to provide informed consent
  • Participation in other clinical trials within the past 30 days
  • Any condition that could interfere with learning and decision-making tasks
  • Known allergies to medications used in the study
  • Significant vision or hearing impairments that could affect task performance
  • History of head trauma or brain injury
  • Inability to follow study instructions or complete required tasks
  • Regular use of psychoactive substances (substances that affect mental processes)
  • Sleep disorders or irregular sleep patterns
  • Serious medical conditions that could affect study participation
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

We usually reply within a few days

Verified sites

All sites with verified contact details – recruitment status may not be available; ask directly

Trial locations

Where you can join this trial

Countries are shaded by recruitment status. Click a recruiting country to ask about joining there.

Not recruiting
Not finding your country?

Not sure what to do next?

Joining a clinical trial can seem overwhelming. We guide you step by step, so you know exactly what to expect and how we support you through the process.

See the full process and FAQ

Investigated drugs

Escitalopram is a medication that belongs to a group called selective serotonin reuptake inhibitors (SSRIs). It works by increasing the amount of serotonin, a chemical messenger, in the brain. In this study, escitalopram is given to participants to see how higher serotonin levels affect their ability to learn new information and make decisions. By comparing people who take escitalopram with those who take a harmless placebo, researchers can learn more about the role of serotonin in everyday thinking and behavior.

What is already known about the treatment

Placebo (microcrystalline cellulose) - The placebo capsule is taken by mouth as a regular tablet. It contains microcrystalline cellulose, an inactive ingredient used as a filler in many pills. It has no therapeutic effect and is not considered a drug, so it is not listed in medical literature as a treatment. It serves only to mimic the appearance of the real medication in the study. Escitalopram - Escitalopram tablets are taken by mouth, usually once daily, and each tablet contains 20 mg of the active ingredient. Escitalopram is an approved antidepressant that is widely used and described in medical research. It works by gently increasing the level of serotonin, a brain chemical that helps regulate mood, by blocking its re‑uptake into nerve cells. It belongs to the class of selective serotonin re‑uptake inhibitors (SSRIs).
Trial detailsLast updated 21 Oct 2026
Age18+ yearsPhasePhase IIITrial ID2024-516055-41-00Estimated enrolment90 patientsSponsorRadboud Universiteit Nijmegen

sourced from the EU Clinical Trials Register and site verification

Want to learn more about this trial or check if you can participate?

Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.