Developing a Web-based Transdiagnostic Single Session Intervention for Patients on Waiting Lists for Psychological Treatment: a Randomized Pilot Feasibility Trial
Sponsor: University of Oslo
Trial Details
| Condition | Depression, Anxiety |
| Intervention | Digital therapy program (short); Digital therapy program (long); Mental health advice |
| Phase | NA |
| Status | Unknown |
| Participants | 80 |
| Est. Completion | 1 Oct 2026 |
| Last Updated | 1 May 2026 |
Primary Outcome
Recruitement rates through the study period as assessed by number of participants providing informed consent, and the time it takes to finish recruitment; Number of participants invited to participate in the study throughout the study period and the frequency of invitations; Number of participants screened for eligibility throughout the study period.; Number of participants in each randomization arm.; Number of responses to each questionnaire and intervention representing missing data patterns and attrition across arms and measurement points; Number of participants who want to pull out of study or get data deleted throughout the study period; Acceptability of interventions and active control conditions as measured by the PFS and TCQ.; Time used to finish questionnaires and interventions; Timing of answers to questionnaires and completion of the study; Belief about positive or negative interaction with planned treatment
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Must have applied for help at The Student Welfare Organization in Oslo and Akershus (SiO Mental Health) through their website. * Must meet SiO Mental health's general eligibility criteria. This includes an individual screening of applications. SiOs general policy is to provide help to all applicants as long as they fulfill the requirement of being a student in the Oslo or Akershus area. * Must speak and write Norwegian. * Internet access and sufficient digital literacy is assumed among the student population. * Willingness to be randomized. * Willingness to partake in the study. * Willingness to have data stored and used for the purpose of the current study. Exclusion Criteria: * No criteria excluding participants who meet the above mentioned inclusion criteria.
Trial Sites
Countries
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