Metabolic Syndrome Clinical Trials

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Multimodal Immersive Virtual Reality Training for Improving Cognition in Adults With Metabolic Syndrome: A Randomized Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to evaluate the effectiveness of a multimodal intervention using immersive virtual reality (Virtual-METS) to improve cognitive function in middle-aged adults with metabolic syndrome and subjective cognitive complaints. The intervention combines cognitive training and physical exercise in group sessions over 12 weeks.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 45
Maximum Age: 70
Healthy Volunteers: f
View:

• Demonstrated criteria for the MetS: central obesity (waist circumference ≥ 94 cm for men or ≥ 80 cm for women) and at least 2 of the criteria described as follow: Triglycerides ≥ 150 mg/dl or specific treatment of this lipid disorder; HDL-C \< 40 mg/dl (men) or \< 50 mg/dl (women) or specific treatment of this lipid disorder; Systolic blood pressure ≥ 130 mmHg or diastolic blood pressure ≥ 85 mmHg or previously diagnosed hypertension treatment; Basal glycemia ≥ 100 mg/dl or type 2 diabetes previously diagnosed).

• Age: between 45 and 70 years old.

• Subjective cognitive complaints: Subjective Cognitive Decline Questionnaire (≥ 7).

• Ability to fully understand and speak Spanish or Catalan.

Locations
Other Locations
Spain
Consorci Sanitari de Terrassa
RECRUITING
Terrassa
Contact Information
Primary
Maite Garolera
mgarolera@cst.cat
+34937310007
Time Frame
Start Date: 2025-03-01
Estimated Completion Date: 2027-04-01
Participants
Target number of participants: 84
Treatments
Experimental: Experimental: Immersive VR-Based Multimodal Intervention (Virtual-METS)
Participants in this arm will receive a multimodal group-based intervention using immersive virtual reality (IVR) without headsets. The intervention includes mindfulness (10 minutes), cognitive training (30 minutes), and physical exercises (20 minutes) delivered through MK360 immersive technology. Sessions are conducted in groups of 5 participants, twice per week for 12 weeks (24 sessions in total), led by a neuropsychologist.
No_intervention: No Intervention: Treatment as Usual (Control Group)
Participants in this arm will continue with their usual care, including routine medical visits and remotely administered psychoeducational guidelines to support diet, physical activity, and adherence to pharmacological treatment. They will not receive any specific intervention during the study period.
Related Therapeutic Areas
Sponsors
Leads: Consorci Sanitari de Terrassa

This content was sourced from clinicaltrials.gov