Effort and Antidepressant Study Test

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-40
SponsorUniversity of Oxford

About this trial

The aim of this study is to investigate the behavioural effects and neural correlates of increasing serotonin levels in healthy volunteers, through a 7-day course of the SSRI escitalopram, on an effort-based decision-making task measuring self-benefiting and prosocial behaviours.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participant is willing and able to give informed consent for participation in the research

Aged 18 to 40 years

Sufficient knowledge of English language to understand and complete study tasks

Right-handed

Disqualifiers

Current or past probable diagnosis of psychiatric illness, according to DSM-5 criteria requiring intervention by a healthcare professional, including but not limited to psychosis, bipolar disorder, major depression, OCD, PTSD, substance abuse disorder or any eating disorder

Current or past diagnosis of any significant personality disorder (e.g., borderline personality disorder) according to self-report

Diagnosis of attention deficit hyperactive disorder or autistic spectrum disorder that impairs daily functioning, requires pharmacotherapy or in the opinion of the study medic would affect the scientific integrity of the study

Current use of medication that might interact with the effects of escitalopram or affect the scientific integrity of the study

Trial design

Design model

Parallel

Treatments tested in this trial

  • Escitalopram 10mg

    Drug

    Escitalopram 10 mg, encapsulated in an opaque capsule to facilitate blinding of participant and researcher

  • Placebo 10 mg

    Drug

    Placebo 10 mg, encapsulated in an opaque capsule to facilitate blinding of participant and researcher

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: EscitalopramExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Effort-based decision-making task for self-benefiting and prosocial behaviours: behavioural correlates

In the fMRI scanner task, participants are prompted to choose between two offers on each trial. One option allows them to earn a low reward for minimal effort (rest), while the other presents a variable higher-reward, higher-effort (work) of the same duration. The low-reward, low-effort offer earns 1 point without exertion. Higher-reward, higher-effort offers range from 2 to 10 points (in 2-point-increments) and effort varies from 30% to 70% (in 10% increments) of their MVC. Each trial differs in whether the outcome is delivered to the participant themselves (self) or someone else (prosocial). Effort levels for each offer are visually represented using coloured portions of a pie chart and rewards (points) are displayed in colour below.

Time frame
Day 7 of treatment
2

Effort-based decision-making for self-benefiting and prosocial behaviours: Neural correlates

Activity of brain regions associated with self-benefiting and prosocial behaviours

Time frame
Day 7 of treatment

Secondary outcomes

1

Emotional processing: Faces task

During the emotional processing face task participants will be presented with pictures of emotional faces and asked to label the emotions into different categories.

Time frame
Day 7 of treatment
2

Prosocial behaviour: Social learning task

This game involves making fictitious investment decisions with other "previous participants in our lab" (programmed responses) and trying to maximize the number of points earned in the game.

Time frame
Day 7 of treatment

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Oxford

Lead sponsor

Wellcome Trust

Collaborator

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