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Multimodal Training With Immersive Virtual Reality to Improve the Cognitive Health and Emotional Well-being of Older Women Living Alone (VirtualDONA)

C

Consorci Sanitari de Terrassa

Status

Not yet enrolling

Conditions

Social Isolation in Older Adults
Poverty

Treatments

Behavioral: VirtualDONA Multimodal Program

Study type

Interventional

Funder types

Other

Identifiers

NCT06956794
2024PROD00053

Details and patient eligibility

About

This study aims to evaluate the effectiveness of an immersive virtual reality-based multimodal intervention (VirtualDONA) to improve cognitive health and emotional well-being in older women living alone and at risk of poverty. The intervention combines mindfulness, cognitive, and physical training in a group format over 8 weeks.

Full description

The VirtualDONA project aims to promote the health of older women living alone and at risk of poverty, as they are considered a highly vulnerable population. Women's longer life expectancy compared to men leads to a greater proportion of women living alone. In Catalonia, there are 786,000 people living alone, and 42.2% are aged 65 or older. The combination of being a woman, of advanced age, and living alone is associated with a high rate of poverty.

These social and economic determinants significantly increase the likelihood of developing dementia and/or mental health disorders in affected individuals. Research has established a connection between social isolation, aging, and a higher probability of experiencing dementia, stress, depression, and anxiety. Economic uncertainty is also known to contribute to stress and anxiety, while social stigma-particularly affecting older women-can negatively impact their cognitive and mental health.

All of these factors highlight the need for preventive interventions targeting women over the age of 65 who live alone and have incomes below the minimum income threshold. VirtualDONA proposes a preventive intervention for this population using immersive virtual reality technology (without headsets) to improve cognitive functioning, emotional well-being, and quality of life.

The intervention will be delivered in a group format over 8 weeks (16 sessions). The combination of mindfulness, cognitive, and physical exercises within a virtual environment offers a suitable multimodal platform for a comprehensive and innovative intervention aimed at vulnerable women. The project aims to demonstrate the benefits of this approach and to develop a sustainable, scalable, and long-term viable business model.

Enrollment

80 estimated patients

Sex

Female

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female
  • Age 65 years or older
  • Living alone
  • Registered with the elderly care services of Suara Cooperativa
  • Annual income below the guaranteed minimum income threshold (below €20,353.62/year)
  • Global cognitive functioning not suggestive of dementia, defined as MMSE score ≥ 24
  • Able to read and write
  • Good command of Catalan and/or Spanish
  • Signed informed consent to participate in the study

Exclusion criteria

  • History of severe neurological, psychiatric disorders, or intellectual disability
  • Uncorrected sensory deficits (e.g., vision or hearing)
  • Physical or motor impairments that may interfere with participation or bias outcome measures

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Immersive VR-Based Multimodal Intervention
Experimental group
Description:
Participants in this arm will receive a multimodal, group-based intervention using immersive virtual reality without headsets. The intervention includes mindfulness, cognitive training, and physical exercises delivered in 16 group sessions over 8 weeks.
Treatment:
Behavioral: VirtualDONA Multimodal Program
Usual Activity (Control Group)
No Intervention group
Description:
Participants in this arm will continue their usual daily routines with no specific intervention during the study period.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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