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Uplift website for depression: feasibility study

Self-help ‘Uplift’ website for depression: a feasibility study of a website using principles of positive psychology for people with symptoms of depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN96366571
Enrollment
100
Registered
2016-05-23
Start date
2016-08-01
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Depression Mental and Behavioural Disorders

Interventions

This intervention comprises a self-help website, containing six activities to promote strengths, positive emotion and social connections for people with depression. The activities in the website are a

Sponsors

East London NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years 2. Have regular access to the internet 3. Have sufficient command of English to complete the measures 4. Endorse one of the Whooley screening items for depression 5. Have capacity to consent

Exclusion criteria

Exclusion criteria: This study has no exclusion criteria as the aim is to be as inclusive as possible. A recent review into how exclusion criteria are used in depression treatment research found that studies excluded between 75-85% of people with depression (Halvorson & Humphreys, 2015). This makes it difficult to generalise from research to the typical clinical population and is something the present study wishes to avoid by having an inclusive sample.

Design outcomes

Primary

MeasureTime frame
The feasibility and acceptability of the intervention will be measured by assessing: 1. Number of website log ins (during six weeks of intervention) 2. Number of times data submitted to the website (during six weeks of intervention) 3. Intervention satisfaction, benefits (after six weeks of intervention)

Secondary

MeasureTime frame
The following outcomes will be measured before the intervention and after 6 weeks of using it in order to assess variability in outcomes and potential for change: 1. Depressive symptoms (PHQ-9) (Kroenke et al., 2001) 2. Life satisfaction (DIALOG) (Priebe et al., 2007)

Countries

England, United Kingdom

Contacts

Public ContactSophie Walsh
sophie.walsh@elft.nhs.uk+44 (0)207 540 4380 (extension 2309)

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026