A randomised evaluation trial of the LIFE FLeX digital health and wellbeing program for anxiety and depression.

Not Applicable

• Conditions: Anxiety; Mental Health - Anxiety; Depressive symptoms; Mental Health - Depression

• Registration Number: ACTRN12617000572369
• Lead Sponsor: Federation University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-04-24
• Study Completion: 2022-03-10
• Last Update Posted: 20 June 2022

Recruitment & Eligibility

• Status: Stopped early
• Sex: All
• Target Recruitment: 67

Inclusion Criteria

Participants must be 18 years or older and concerned about their anxiety and or depressive symptoms.

LIFE FLeX has been developed for people with depressive and anxiety symptoms and therefore recruitment will focus on people with depression and anxiety. However, those without symptoms are able to register if they wish too. The program is also preventative in nature and therefore non-anxious and/or depressed participants may also benefit from some of the information within the program (e.g., increasing wellness flexibility).

Exclusion Criteria

No internet access, does not create a My Digital Health account (requires the provision of a valid email address), does not provide consent to study conditions.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depressive symptoms using the PHQ-9[Pre-intervention, during intervention (Week 3 and 5), post and 1 and 3 month follow-up];Anxiety symptoms using the GAD-7 [Pre-intervention, during intervention (Week 3 and 5), post and 1 and 3 month follow-up];Emotional dysregulation by using the DERS-Brief[Pre-intervention, post and 1 and 3 month follow-up]