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Feasibility and Efficacy of a Digital Training Intervention to Increase Reward Sensitivity- Imager

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05623826
Acronym
IMAGER
Enrollment
137
Registered
2022-11-21
Start date
2020-09-27
Completion date
2021-04-13
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Keywords

stress, health, resilience

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.

Interventions

OTHERCognitive- behavioral imagery-based training

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.

Sponsors

Johannes Gutenberg University Mainz
CollaboratorOTHER
Radboud University Medical Center
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
CollaboratorOTHER
University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, 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.

Intervention model description

Parallel group design with control group completing only EMA, not EMI

Eligibility

Sex/Gender
ALL
Age
18 Years to 29 Years
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

Design outcomes

Primary

MeasureTime frameDescription
Behavioural avoidance/inhibition (BIS/BAS) scalesone week: Pre- to post-intervention/controlSelf-reported reward sensitivity, scale range \[0-15\], higher score = worse outcome
The Sensitivity to Punishment and Sensitivity to Reward Questionnaire (SPSRQ)one week: Pre- to post-intervention/controlSelf-reported reward sensitivity, scale range \[0-24\], higher score = better outcome
Perceived Stress Scale (PSS)one week: Pre- to post-intervention/controlSelf-reported level of stress, scale range \[0-40\], higher score = worse outcome
Beck Depression Inventory II (BDI-II)one week: Pre- to post-intervention/controlSelf-reported depressive symptoms, scale range \[0-63\], higher score = worse outcome
State-Trait Anxiety Inventory (STAI)one week: Pre- to post-intervention/controlSelf-reported anxiety symptoms, scale range \[20-80\], higher score = worse outcome

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026