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Digital Self-efficacy Training to Bridge Waiting Times for Psychotherapy

Digital Self-efficacy Training to Bridge Waiting Times for Psychotherapy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05560581
Enrollment
94
Registered
2022-09-29
Start date
2022-11-07
Completion date
2025-11-30
Last updated
2025-03-04

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

Conditions

Psychiatric Disorder, Waiting for Psychotherapy

Brief summary

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.

Interventions

BEHAVIORALDigital self-efficacy training

Prior to the app participation, participants will receive psychoeducation on self-efficacy and will be instructed to define two autobiographical self-efficacy memories (own achievements, e.g., completion of an exam, success in a sporting event). During the week of app participation, they will be prompted three times per day and asked to perform an imagination task. Step by step, they will recall one of their autobiographic self-efficacy memories and focus on their character traits and abilities that were relevant for their achievement.

Participants will receive questions on mood and social/virtual contacts 3 times per day.

Sponsors

Psychiatric University Hospital, Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

double-blind

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in self-efficacybaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganValidated measures (General Self-Efficacy Scale (10 items; higher scores indicate higher self-efficacy -\> better outcome), Coping Self-efficacy scale (26 items; higher scores indicate higher self-effiacy -\> better outcome) and individual questions based on validated measures assessing specific self-efficacy regarding emotion regulation, therapy and waitlist will be used to assess self-efficacy at baseline and 3 different time points after the intervention.

Secondary

MeasureTime frameDescription
Change in stressbaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganStress will be assessed using the validated measure Perceived Stress Scale (10 items; higher scores indicate greater stress -\> worse outcome).
Change in depressionbaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganDepression will be assessed using the validated measure Beck Depression Inventory II (21 items; higher scores indicate greater depression -\> worse outcome).
Change in optimismbaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganChange in life orientation will be assessed using the validated measure Life Orientation Test Revised (10 items; higher scores indicate greater optimism -\> better outcome)
Change in intolerance of uncertaintybaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganIntolerance of uncertainty will be assessed using the validated measure Intolerance of uncertainty scale (18 items; higher scores indicate greater uncertainty -\> worse outcome).
Change in hopelessnessbaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganHopelessness will be assessed using the validated measure Beck Hopelessness Scale (20 items; higher scores indicate greater hopelessness -\> worse outcome).
Change in anxietybaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganAnxiety will be assessed using the validated measure State and Trait Anxiety Scale (40 items; higher scores indicate greater anxiety -\> worse outcome).
Change in therapy expectationsbaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganTherapy expectations will be assessed using the validated measure Patient Questionnaire on Therapy Expectation and Evaluation (11 items; higher score indicates higher satisfaction -\> better outcome).

Other

MeasureTime frameDescription
Motivation and life enjoymentbaseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy beganAdditional questionnaire with single items assessing therapy motivation and life enjoyment with items based on the validated questionnaires Quality of Life Enjoymend and Satisfaction Questionnaire, Fragebogen zur Psychotherapiemotivation und Fragebogen zur Messung der Psychotherapiemotivation
Change in mood and contacts3 per day during one-weekpos. and neg. mood and contacts will be assessed with the Ecological Momentary Assessment. Higher pos. mood / lower neg. mood -\> better outcome
Change in in ability to workbaseline to 1 month after the intervention, within 1 month after the subsequent therapy beganWe will ask about the participants' self-evaluation at baseline and 2 different time points after the intervention (self-evaluation; no specific score will be used)

Countries

Switzerland

Contacts

Primary ContactJudith Rohde, MD
judith.rohde@uzh.ch+41 (0)58 384 65 00

Outcome results

None listed

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