Clinical Trials Directory

Trials / Completed

CompletedNCT05812729

"resiLIR Basic": A Psychological Online Intervention to Enhance Resilience in the General Population

A Randomized Controlled Study to Evaluate the Feasibility and Efficacy of an Online Resilience Intervention in the General Population ("resiLIR Basic")

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
244 (actual)
Sponsor
Leibniz-Institut für Resilienzforschung (LIR) gGmbH · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to examine the developed online resilience intervention "resiLIR Basic" for the general population. Participants will receive a 6-week online intervention addressing resilience and stress as well as different resilience factors. The main question is whether the intervention is effective in increasing psychological resilience.

Detailed description

Background: Acute and chronic stress in everyday life plays an essential role in the onset and development of several physical and mental health conditions. The ability to maintain or return to mental health during stress exposure is characterized as resilience. Especially the COVID-19 pandemic emphasized the role of resilience for mental health and pointed to the importance of easily accessible and flexible interventions to improve resilience in the general population. Objectives: The aim of the study therefore is to examine the feasibility and efficacy of a newly developed online intervention to foster resilience in the general population. Methods: In a waitlist control design, 240 adults will participate in the 6-week resilience intervention "resiLIR Basic". This online intervention consists of 8 modules of about 45-60 minutes length using psycho-educational elements and practical exercises to address evidence-based resilience factors, such as optimism or sense of coherence. Participants will complete online surveys on resilience, mental health, and several resilience factors pre-, during and post-intervention as well as 3, 6 and 12 months after completion as follow-up assessments. Implications: The study will contribute to an evidence-based and easily accessible supply of resilience interventions supporting health promotion and stress prevention in the general population.

Conditions

Interventions

TypeNameDescription
BEHAVIORALresiLIR BasicEach module contains psychoeducational elements as well as practical exercises. Week 1: Introduction + "Stress and resilience" Week 2: "Optimism" Week 3: "Mindfulness" Week 4: "Sense of coherence and values" Week 5: "Acceptance" Week 6: "Self-compassion" + Conclusion

Timeline

Start date
2023-06-14
Primary completion
2024-06-28
Completion
2024-06-28
First posted
2023-04-14
Last updated
2024-10-23

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT05812729. Inclusion in this directory is not an endorsement.