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NCT07793097Not yet recruiting

Can Mindfulness and Virtual Reality Reduce Stress in Young Adults With Type 1 Diabetes?

Feasibility of MBSR-VR to Reduce Stress Among Emerging Adults With T1D

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

The goal of this study is to learn if Mindfulness-Based Stress Reduction (MBSR) can be delivered using virtual reality (VR) technology to emerging adults (youth 16-20 years old) with type 1 diabetes and high levels of stress reactivity. If successful, MBSR-VR has the potential to reach many people who may be living in different places who might not have access to programs like MBSR. This is important because young adults with a chronic illness like diabetes and high levels of stress have been shown to have worse health than young adults with lower stress and young adults without diabetes. This study has not been designed to determine if MBSR-VR improves the health of young adults with diabetes (improves their glycemic control),their feelings of distress (this includes stress, depression, and anxiety), or their mindfulness (being more aware of their thoughts, feelings, actions, and environment) but we will look to see if people are reporting improvements in these areas.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
48 (estimated)
First submitted
11 Aug 2026
Start date
31 Oct 2026
Primary completion date
1 May 2028
Lead sponsor
Wayne State University
NCT number
NCT07793097

What you commit to

  • Study type: Interventional
  • Planned participants: 48
  • From 31 Oct 2026 to the primary completion date, 1 May 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Significant co-morbid mental health problems limiting the participant's ability to engage effectively in the group nature of the intervention (i.e., thought disorders like schizophrenia, severe cognitive impairment, suicidality or homicidality)
  • Co-morbid physical health problems in which diabetes is secondary to another chronic medical illness (e.g., cystic fibrosis) and their medical management differs substantially from that of most youth with T1D

Other

  • Non-English fluency

Who the study is looking for

  • Age 16 to 20 years, inclusive
  • Diagnosed with type 1 diabetes (T1D) for at least six months
  • Have elevated levels of stress reactivity as assessed by the Perceived Stress Reactivity Scale (PSRS)
  • Access to an internet-enabled device on which the participant can participate in virtual study activities

Age in the registry: 16 years to 20 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Johns Hopkins University
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
Wayne State University
Coordinator of this site? Confirm its status
DetroitUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.