Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Two-week smartphone program to boost reward response in people with anhedonia

Official title: Ecological Momentary Intervention for Reward in Anhedonia

Run by Philipps University Marburg · NCT07155941 · Data updated 2026-11-12

This trial tests whether three brief daily smartphone audio exercises teaching positive imagery, savoring, gratitude, and related skills can reduce anhedonia and psychological distress in German-speaking adults with elevated anhedonia and depression.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorPhilipps University Marburg
Academic / other
Locations1 site (Marburg, Hesse)
StatusRecruiting
StartedJune 18, 2025
Main results expectedJanuary 2026
Study endsJanuary 2026
Registry record updatedJanuary 9, 2026
Trial IDNCT07155941 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

German-speaking adults who own a smartphone and have clinically elevated anhedonia (SHAPS ≥ 25) and elevated depression (DASS-21-Depression ≥ 10) plus elevated anxiety or stress, and who are not on psychotropic medication or in psychotherapy, are ideal candidates.

Probably not a fit

People taking psychotropic medications, currently in or planning psychotherapy, or with suicidality, bipolar disorder, or psychotic episodes are excluded and unlikely to benefit from this brief app-based intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Participants are assigned to either an experimental ecological momentary intervention (three daily audio exercises targeting reward anticipation, consumption, and learning) or an active control (progressive muscle relaxation) delivered via a smartphone app over two weeks. Exercises include positive mental imagery, savoring, taking ownership of positive experiences, gratitude, and cognitive reframing, designed to strengthen reward processing. Key eligibility requires clinically elevated anhedonia (SHAPS ≥ 25) and elevated depression (DASS-21-Depression ≥ 10) plus elevated anxiety or stress, with exclusions for psychotropic medication, ongoing/planned psychotherapy, suicidality, bipolar disorder, or psychosis. Outcomes focus on changes in anhedonia and related depressive, anxiety, and stress symptoms following the two-week intervention.

Why it matters

Potential benefit: If successful, the intervention could quickly increase pleasure and motivation and reduce depressive and anxiety symptoms through a low-cost, accessible smartphone program.

How similar studies have gone: Component-based positive affect interventions such as Positive Affect Treatment have shown promising early results, but fully smartphone-delivered ecological momentary interventions for anhedonia are relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* German speaking
* Smartphone available and willingness to participate in repeated training units and questions delivered via app
* Clinically elevated anhedonia (SHAPS \>= 25) and elevated depression (DASS-21-Depression \>= 10), elevated anxiey (DASS-21-Anxiety \>= 6) or elevated stress (DASS-21-Stress \>= 10)

Exclusion Criteria:

* Psychotropic medication
* Psychotherapy currently ongoing or planned during participation
* Suicidality, lifetime diagnosis of bipolar disorders or psychotic episodes

Where it's running

  • Philipps-University Marburg
    Marburg, Hesse, Germany
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.