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Digital Self-efficacy Training to Bridge Waiting Times for Psychotherapy

P

Psychiatric University Hospital, Zurich

Status

Enrolling

Conditions

Psychiatric Disorder
Waiting for Psychotherapy

Treatments

Behavioral: Digital self-efficacy training
Behavioral: Ecological Momentary Assessment

Study type

Interventional

Funder types

Other

Identifiers

NCT05560581
SeApp III

Details and patient eligibility

About

The main aim of this project is to improve waiting periods for specialised psychotherapy. We will apply a brief, smartphone-based self-efficacy training to patients with psychiatric disorders waiting for specialised psychotherapy. Additionally, we will use Ecological Momentary Assessment (EMA) to assess mood, social contacts, and other parameters daily. We will investigate whether the training can improve self-efficacy and related constructs and if it can help reduce stress and waitlist drop-outs during waiting periods. Additionally, we will investigate if the self-efficacy training has a positive effect on motivation and therapeutical relationship regarding the subsequent therapy.

After a screening for eligibility, participants will be randomly assigned to intervention and control group. At baseline, participants attend a laboratory session where they are assessed for current psychiatric disorders and further relevant psychological variables. They will then either participate in the digital self-efficacy training combined with EMA (intervention group) or in EMA only (control group). Both will be conducted via a smartphone app. Subsequently, participants will be asked to fill in post questionnaires at three different time points: after having finished app usage, one month later, and after the beginning of the subsequent psychotherapy.

Enrollment

94 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • psychiatric disorder
  • age 18-65
  • waiting for psychiatric assessment/treatment (being on waitlist)
  • sufficient knowledge of the German language
  • smartphone user
  • internet access via smartphone
  • internet access at home (laptop, tablet, or computer)

Exclusion criteria

  • current intense psychotherapy
  • acute suicidality
  • acute psychotic symptoms
  • substance addiction

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

94 participants in 2 patient groups

Intervention group
Experimental group
Description:
Participants will receive an one-week digital self-efficacy training (3x/day) and an one-week Ecological Momentary Assessment (3x/day questions on mood, social and virtual contacts).
Treatment:
Behavioral: Ecological Momentary Assessment
Behavioral: Digital self-efficacy training
Control group
Active Comparator group
Description:
Participants will receive an one-week Ecological Momentary Assessment (3x/day questions on mood, social and virtual contacts).
Treatment:
Behavioral: Ecological Momentary Assessment

Trial contacts and locations

2

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Central trial contact

Judith Rohde, MD

Data sourced from clinicaltrials.gov

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