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OxIGen: Oxford Imagery Generation: Investigating the Effects of an Internet Based Computer Program in Depression

OxIGen: Oxford Imagery Generation: Investigating the Effects of an Internet Based Computer Program in Depression

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01443234
Acronym
OxIGen
Enrollment
150
Registered
2011-09-29
Start date
2012-02-29
Completion date
2013-12-31
Last updated
2014-01-09

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

Conditions

Depression

Keywords

Depression, Cognitive Bias, Internet

Brief summary

This research study is designed to investigate the effects of an online computer program, called OxIGen (Oxford Imagery Generation), on thinking style and mood in depression. The OxIGen program will be delivered online over four weeks and with follow-up at one, three and six months. This will inform potential future development of this computerized task into an online intervention to modify negative thinking styles in depression.

Interventions

OTHEROxIGen

Internet-based intervention with 12 sessions over 4 weeks

OTHEROxIGen: control version

A control version of the OxIGen internet-based intervention (i.e. identical but with putative active components removed)

Sponsors

Lupina Foundation
CollaboratorUNKNOWN
University of Oxford
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Willing and able to give consent to the study * Male or Female, aged between 18 and 65 years * Current Major Depressive Episode (assessed by semi-structured clinical interview) * Access to internet in order to complete the online program * Able to travel to research centre for assessment appointments * Fluent in written and spoken English

Exclusion criteria

* Meets criteria for current psychotic disorder * History of mania or hypomania as assessed by semi-structured clinical interview, or has elsewhere received a diagnosis of Bipolar disorder * Antidepressant medication begun or changed in dosage during last month * Meets criteria for current substance abuse disorder * Involved in other current treatment trials * Currently receiving psychological therapy

Design outcomes

Primary

MeasureTime frame
Change in score on Beck Depression Inventory - IIBaseline and post-intervention (4 weeks)

Secondary

MeasureTime frameDescription
Change on EuroQol-5DBaseline and Post-Intervention (4 weeks)
Change in NeuroticismBaseline and Post-Intervention (4 weeks)
Change on Beck Depression Inventory - IIBaseline and Follow-Up (one month, three months, six months)
Change in score on Quick Inventory of Depressive Symptoms - Self ReportBaseline and post-intervention (4 weeks)
Change in State-Trait Anxiety Inventory (Trait scale)Baseline and Post-Intervention (4 weeks)
Change on Beck Anxiety InventoryBaseline and Post-Intervention (4 weeks)
Change on Scrambled Sentences TaskBaseline and Post-Intervention (4 weeks)
Change on Life Orientation Test - RevisedBaseline and Post-Intervention (4 weeks)
Change on Prospective Imagery TestBaseline and Post-Intervention (4 weeks)
Change on Behavioural Activation in Depression ScaleBaseline and Post-Intervention (4 weeks)
Change in IAPT ToolkitBaseline and Post-Intervention (4 weeks)Includes the GAD-7, PHQ-9 and Work and Social Adjustment Scale
Change on Quick Inventory of Depressive Symptoms - Self ReportBaseline and Follow-Up (one month, three months, six months)
Change on State-Trait Anxiety Inventory (Trait scale)Baseline and Follow-Up (one month, three months, six months)
Change on IAPT ToolkitBaseline and Follow-Up (one month, three months, six months)Includes GAD-7, PHQ-9, Work and Social Adjustment Scale
Change on Euroqol-5DBaseline and Follow-Up (one month, three months, six months)
Change on NeuroticismBaseline and Follow-Up (one month, three months, six months)
Image Generation TaskPost-Intervention (4 weeks)Task adapted from Sharot et al. (2007, Nature)

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026