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A randomised controlled trial and consumer characteristics of the Stress eHealth wellbeing program.

The evaluation of the Stress eHealth wellbeing program in decreasing anxiety, depressive and stress symptoms in adults: A randomised controlled trial.

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614001308684
Enrollment
107
Registered
2014-12-16
Start date
2014-12-22
Completion date
2015-12-30
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This project will involve trialling a multi-component online stress reduction program (Stress eHealth) designed to reduce stress and anxiety and improve mental and physical wellbeing. Those that consent will be randomly allocated to the Stress eHealth program (immediate access group) or a wait control group (delayed access group). The delayed access group will receive the intervention following a 10-week waiting period. Participants randomised to the Stress eHealth (immediate access) group will complete a pre-intervention assessment (Week 0), during intervention (Weeks 1-5) assessment, post-intervention assessment (Week 6) and a 1 and 3 month follow-up assessment (Week 10 & Week 18). Participants randomised to the delayed access group will complete the same assessment phases, except for the 3 month follow-up assessment, as they will be given access to Stress eHealth program following the 1 month follow-up assessment (Week 10). However the delayed access group will be asked to complete the post intervention assessment after they complete the Stress eHealth program (Week 16).

Interventions

A simple randomised controlled trial (RCT) design will be used to evaluate the effectiveness of a multi-component online program for decreasing stress and improving mental and physical wellbeing (called Stress eHealth). The Stress eHealth program is placed within the Federation University eHealth Platform, which is a platform. People who visit the website, either directly or through seeing the program advertised, will be invited to take part in the Stress eHealth evaluation study. Those that c

A simple randomised controlled trial (RCT) design will be used to evaluate the effectiveness of a multi-component online program for decreasing stress and improving mental and physical wellbeing (called Stress eHealth). The Stress eHealth program is placed within the Federation University eHealth Platform, which is a platform. People who visit the website, either directly or through seeing the program advertised, will be invited to take part in the Stress eHealth evaluation study. Those that consent will be randomly allocated to the Stress eHealth program (immediate access group) or a wait control group (delayed access group). The delayed access group will receive the intervention following a 10-week waiting period. Stress eHealth contains five modules, delivered weekly over the five weeks, and is designed to help people cope with challenging situations and enhance their mental and physical wellbeing. Each module will take between 10-20 minutes to complete. Participants will also receive automated emails (e.g., to remind them to log on, when to complete post/follow-up questionnaires) and will be asked several questions at the beginning of each week, to monitor their progress. Stress eHealth has five modules: 1. Stress and Health 2. Your Thoughts 3. Relaxation and Physical Activity 4. Social Connectedness and Strengths 5. Mindfulness Participants randomised to the Stress eHealth (immediate access) group will complete a pre-intervention assessment (Week 0), during intervention (Week 1-5) assessment, post-intervention assessment (Week 6) and a 1 and 3 month follow-up assessment (Week 10 & Week 18). The will have access the Stress eHealth program for the entire duration of the study. Those randomly allocated to the waitlist condition will be asked to complete the same assessment phases, except for the 3 month follow-up assessment, as they will be given access to Stress eHealth program following the 1 month follow-up assessment (Week 10). However the delayed access group will be asked to complete the post intervention assessment after they complete the Stress eHealth program (Week 16).

Sponsors

Federation Unversity
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants must be 18 years or older, have access to the internet, be able to register online using an email address and consent to the the study.

Exclusion criteria

There are no key exclusion criteria.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026