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Social AnxietyNCT06977087

The Efficacy of Prospective Mental Imagery in Enhancing Approach Motivation Among Socially Anxious Individuals

A study testing Psychoeducation, Prospective Mental Imagery and Verbal Reasoning in people with Social Anxiety and Social Phobia, run by Philipps University Marburg at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The efficacy of an online intervention aimed at enhancing approach motivation and behavioral engagement in confronting anxiety-inducing social situations is examined among individuals with elevated social anxiety. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Social Anxiety, Social Phobia
What is being tested?
Psychoeducation, Prospective Mental Imagery and Verbal Reasoning
Could I receive a placebo?
No, everyone receives an active treatment
How many people
129 participants
Where
1 siteGermany
Study dates
4 Mar 2025to 1 Jul 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Elevated score on Mini-Social Phobia Inventory (Mini-SPIN) > 6
  • Moderate fear and avoidance of two specified social situations (i.e., giving a stranger a compliment and asking for a restaurant recommendation), each rated above 5 on a Likert scale ranging from 0 (not at all) to 10 (extremely), respectively
  • Avoidance of the two specified social situations (i.e., giving a stranger a compliment and asking for a restaurant recommendation), indicated by not having engaged in either behaviors in the past 7 days

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Germany Philipps University

    Marburg, 35037

Other trials in Germany

About this study

Official title: The Efficacy of Prospective Mental Imagery in Enhancing Approach Motivation Among Socially Anxious Individuals: A Randomized Controlled Trial

The efficacy of an online intervention aimed at enhancing approach motivation and behavioral engagement in confronting anxiety-inducing social situations is examined among individuals with elevated social anxiety. Participants will receive psychoeducation, followed by either a prospective mental-imagery task or a verbal reasoning task. Efficacy of the intervention is measured by ratings of experienced and anticipated pleasure, approach motivation and self-reported engagement with feared situations one week later.

Read the detailed description

With numerous studies demonstrating its long-term effectiveness, exposure therapy is currently considered the leading evidence-based treatment for anxiety disorders. However, a major limitation in its application is that patients often discontinue treatment due to their unwillingness to confront themselves with the feared situation. Considering that targeting avoidance behaviors and maladaptive fear responses are at the core of exposure therapy, strategies are needed to enhance both approach motivation as well as behavioral engagement with the feared situation. Among individuals with depression, prospective mental imagery has been demonstrated to increase motivation and behavioral engagement in pleasurable activities by elevating anticipated reward as well as anticipatory and anticipated pleasure ('motivational amplifier' hypothesis). Given alterations in motivational and reward processes in individuals with social anxiety, prospective mental imagery may enhance reward anticipation and facilitate approach motivation and engagement in exposure to socially feared situations. The current online study will compare the use of a prospective mental-imagery task to an active control group (verbal reasoning) in improving approach motivation and behavioral engagement with feared situations in individuals with heightened social anxiety. Participants in both conditions will receive psychoeducation. Participants in the experimental group will vividly imagine themselves successfully mastering the feared social situation. Participants in the control condition are asked to reflect on the pros and cons of confronting themselves with the feared social situation. Approach motivation as well as reward anticipation, anticipated and anticipatory pleasure will be assessed before and after the imagery or verbal reasoning task. Engagement with the feared social situation will be assessed one week later. Aim of the randomized controlled trial is to investigate whether prospective mental imagery is effective in enhancing self-reported motivation and engagement with feared situations compared to an active control group. In an exploratory analysis, we will examine whether the efficacy of the prospective imagery training is modulated by individuals' levels of reward sensitivity and anhedonia.

Being tested
Psychoeducation, Prospective Mental Imagery, Verbal Reasoning
Medical subject headings
Phobia, Social

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PsychoeducationBehavioural

    Providing information about social anxiety, role of safety and avoidance behaviors in maintaining social anxiety, rationale for exposure to feared social situations

  • Prospective Mental ImageryBehavioural

    A standard imagination script is recounted in which participants have successfully mastered the socially feared situation

  • Verbal ReasoningBehavioural

    Participants are asked to reflect on the pros and cons of facing the socially feared situation

Study groups in NCT06977087
Study groupRoleWhat they receive
Psychoeducation + Prospective Mental-Imagery TaskExperimentalProspective mental imagery of post-exposure experience
Receives: Behavioral: Psychoeducation; Behavioral: Prospective Mental Imagery
Psychoeducation + Verbal Reasoning TaskActive comparatorVerbal reasoning of pro and cons of exposure
Receives: Behavioral: Psychoeducation; Behavioral: Verbal Reasoning

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anticipatory Pleasure

    2-item questionnaire on a scale 0 (not at all) to 100 (extremely) assessing current pleasure when imaging approaching and having approached the feared situations.

    Measured: Baseline (prior to the assigned intervention) and immediately post-intervention (following the prospective mental imagery or verbal reasoning task)

  2. Anticipated Pleasure

    2-item questionnaire on a scale 0 (not at all) to 100 (extremely) assessing expected pleasure when approaching and having approached the feared situations.

    Measured: Baseline (prior to the assigned intervention) and immediately post-intervention (following the prospective mental imagery or verbal reasoning task)

  3. Reward Anticipation

    2-item questionnaire on a scale 0 (not at all) to 100 (extremely) assessing expected reward related to approaching and having approached the feared situations.

    Measured: Baseline (prior to the assigned intervention) and immediately post-intervention (following the prospective mental imagery or verbal reasoning task)

  4. Motivation

    Self-reported motivation to approach the feared situations on a scale of 0 (not at all) to 100 (extremely).

    Measured: Baseline (prior to the assigned intervention) and immediately post-intervention (following the prospective mental imagery or verbal reasoning task)

  5. Frequency of Exposure

    Self-reported frequency of exposure to the feared situations.

    Measured: Post-treatment (i.e., 7 days after baseline)

Secondary outcomes (9)
  1. Social Phobia Inventory (SPIN)

    17-item questionnaire on a 5-point Likert scale (0 = 'not at all'; 4 = 'extremely') assessing symptom severity related to social anxiety (i.e., fear, avoidance, physical symptoms). Total range score: 0 to 68. Higher scores indicating greater severity of social anxiety.

    Measured: Change from baseline to post-treatment (i.e., 7 days)

  2. Mood State Questionnaire

    6-item assessment using a 7-point bipolar Likert scale to measure a person's current mood across three dimensions: energetic arousal, valence, and calmness. Higher scores indicating higher energetic arousal, more positive valence, and greater calmness.

    Measured: Baseline (prior to the assigned intervention) and immediately post-intervention (following the prospective mental imagery or verbal reasoning task)

  3. Liebowitz Social Anxiety Scale (LSAS)

    24-item questionnaire on a 4-point Likert scale (fear: 0 = 'none'; 3 = 'severe'; avoidance: 0 = 'never'; 3 = 'usually') assessing both fear/anxiety and avoidance of social situations, respectively. Total range score: 0 to 144. Higher scores indicating greater fear and avoidance as well as severity of social anxiety.

    Measured: Change from baseline to post-treatment (i.e., 7 days)

  4. Patient Health Questionnaire-9 (PHQ-9)

    9-item questionnaire on a 4-point Likert scale (0 = 'not at all'; 3 = 'nearly every day') assessing the presence and severity of depressive symptoms. Total range score: 0 to 27. Higher scores indicating more severe depression.

    Measured: Baseline

  5. Positive and Negative Affect Schedule (PANAS)

    20-item questionnaire on a 5-point Likert scale (0 = 'not at all'; 4 = 'extremely') assessing the presence and intensity of both positive and negative emotions. Total score range for positive affect (PA) and negative affect (NA), respectively: 0 to 50. Higher scores indicate on either scale indicate a higher level of that emotion.

    Measured: Baseline

  6. Snaith-Hamilton-Pleasure-Scale (SHAPS)

    14-item questionnaire on a 4-point Likert scale (0 = 'strongly disagree'; 3 = 'strongly agree') measuring anhedonia. Total score range: 0 to 42. Higher total scores indicate greater levels of anhedonia.

    Measured: Baseline

  7. Positive Valence System Scale (PVSS-21)

    21-item questionnaire on a 9-point Likert scale (1= 'extremely untrue of me'; 9 = 'extremely true of me') assessing an individual's response to various types of rewards in daily life. Total score range: 21 to 105. Higher scores indicating a greater tendency to experience pleasure and respond to rewards.

    Measured: Baseline

  8. Vividness of Mental Imagination

    Vividness of imagination on a scale from 0 (not at all) to 100 (extremely vivid) assessed immediately after prospective mental-imagery and verbal reasoning task.

    Measured: Immediately after assigned interventions (prospective mental imagery and verbal reasoning task) at baseline

  9. Verbal Reasoning

    Intensity of reflection on the pros and cons of seeking out the feared situation on a scale from (not intensive at all) to 100 (extremely intensive) assessed after prospective mental-imagery and verbal reasoning task.

    Measured: Immediately after assigned interventions (prospective mental imagery and verbal reasoning task) at baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2025
  2. Study start4 Mar 2025
  3. Primary completion1 Jul 2026
  4. Study completion1 Jul 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
129 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06977087
Sponsor's protocol ID
Trau dich! 2.0
Status last verified
Jul 2026
First submitted
30 Apr 2025
Last updated
7 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Hallford DJ, Farrell H, Lynch E. Increasing anticipated and anticipatory pleasure through episodic thinking. Emotion. 2022 Jun;22(4):690-700. doi: 10.1037/emo0000765. Epub 2020 Jun 18.

    PubMed 32551746
  • Renner F, Werthmann J, Paetsch A, Bar HE, Heise M, Bruijniks SJE. Prospective Mental Imagery in Depression: Impact on Reward Processing and Reward-Motivated Behaviour. Clin Psychol Eur. 2021 Jun 18;3(2):e3013. doi: 10.32872/cpe.3013. eCollection 2021 Jun.

    PubMed 36397959
  • Renner F, Murphy FC, Ji JL, Manly T, Holmes EA. Mental imagery as a "motivational amplifier" to promote activities. Behav Res Ther. 2019 Mar;114:51-59. doi: 10.1016/j.brat.2019.02.002. Epub 2019 Feb 5.

    PubMed 30797989
  • Ji JL, Geiles D, Saulsman LM. Mental imagery-based episodic simulation amplifies motivation and behavioural engagement in planned reward activities. Behav Res Ther. 2021 Oct;145:103947. doi: 10.1016/j.brat.2021.103947. Epub 2021 Aug 15.

    PubMed 34433114

Questions about this trial

What is this clinical trial studying?

A study testing Psychoeducation, Prospective Mental Imagery and Verbal Reasoning in people with Social Anxiety and Social Phobia, run by Philipps University Marburg at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anticipatory Pleasure (time frame: Baseline (prior to the assigned intervention) and immediately post-intervention (following the prospective mental imagery or verbal reasoning task)). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06977087, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jul 2026.

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