Skip to main content
Clinical Trials/NCT05623826
NCT05623826CompletedNot Applicable

Feasibility and Efficacy of Imager, a Digital Training Intervention to Increase Reward Sensitivity: A Randomised Controlled Trial

University of Zurich1 site in 1 country137 target enrollmentStarted: September 27, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
137
Locations
1
Primary Endpoint
State-Trait Anxiety Inventory (STAI)

Study Overview

Brief Summary

Development and feasibility test of an Ecological Momentary Intervention (EMI) - Imager, to promote and improve stress resilience, specifically to increase reward sensitivity.

Detailed Description

Aim of the current project is to develop and test Ecological Momentary Intervention (EMI) - Imager, to promote and improve stress resilience, specifically to increase reward sensitivity. EMIs are mostly smartphone-based applications that deliver interventions to people as they go about in their daily lives. The EMI developed and tested here is based on theoretical and empirical findings and consists of several items and a repeated training using various individual scenarios from participants' life that will be presented to participants via an app on their smartphones.

This study tests the feasibility and effects of the EMI on a change in (i) reward sensitivity, (ii) mental imagery, and (iii) indices of perceived stress. One hundred twenty healthy student participants, aged 18-29 will be included in the study. Participants will be screened first and included if they score 5 points or more on the Reward Sensitivity Subscale of Behavioral Avoidance/Inhibition (BIS/BAS) scales. This is necessary in order to avoid a ceiling effect. Then, participants will be randomly assigned to an experimental (reward sensitivity EMI) or two of the control conditions (control EMA or waitlist). The reward sensitivity EMI group will be taught about experiencing rewards in daily life and will be asked to apply the specific techniques to personal situations repeatedly. The control EMA group will use the same app consisting of Ecological Momentary Assessment only, and the waitlist group will not receive any mobile app.

The training will last seven consecutive days and the app will send (i) 10 prompts per day to ask about the current mood of the user in control EMA and experimental groups and (ii) three prompts per day resulting in a total of 21 reward training sessions only in the experimental group. Participants will be able to use a special button triggering the intervention or EMA by themselves too. After one week, participants will return to the lab, fill in questionnaires and participate in behavioral tasks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Outcomes Assessor)

Masking Description

Participants are informed of the two group design, individual group allocation is released to participants at the end of the study participation.

Eligibility Criteria

Ages
18 Years to 29 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •being a student
  • •having sufficient knowledge of the German language
  • •being a smartphone user
  • •score of 5 points or more in Reward Sensitivity Subscale of Behavioral Avoidance/Inhibition (BIS/BAS) scales

Exclusion Criteria

  • •having a mental illness or attending the psychotherapy

Arms & Interventions

Experimental

Experimental

Experimental (receiving EMA and Imager EMI)

Intervention: Cognitive- behavioral imagery-based training (Other)

Control

No Intervention

Control (receiving EMA only)

Outcomes

Primary Outcomes

State-Trait Anxiety Inventory (STAI)

Time Frame: one week: Pre- to post-intervention/control

Self-reported anxiety symptoms, scale range \[20-80\], higher score = worse outcome

The Sensitivity to Punishment and Sensitivity to Reward Questionnaire (SPSRQ)

Time Frame: one week: Pre- to post-intervention/control

Self-reported reward sensitivity, scale range \[0-24\], higher score = better outcome

Behavioural avoidance/inhibition (BIS/BAS) scales

Time Frame: one week: Pre- to post-intervention/control

Self-reported reward sensitivity, scale range \[0-15\], higher score = worse outcome

Beck Depression Inventory II (BDI-II)

Time Frame: one week: Pre- to post-intervention/control

Self-reported depressive symptoms, scale range \[0-63\], higher score = worse outcome

Perceived Stress Scale (PSS)

Time Frame: one week: Pre- to post-intervention/control

Self-reported level of stress, scale range \[0-40\], higher score = worse outcome

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials