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UnknownNCT04804800

Experimental group 1 : Virtual Reality for Eating disorders; Dysmorphophobia

This study has an unknown status. It is testing Experimental group 1 : Virtual Reality for Eating disorders; Dysmorphophobia.

Body dysmorphic disorder, Eating disorders, ...BehavioralFrom 15 Years to 26 Years

Current recruitment is not confirmed. Check the official registry or contact the research team before making plans to participate.

Then choose your country and confirm availability with each study site.

In plain English

Key information made simple

What is this study testing?

This study is testing whether a digital tool or app may be useful for people experiencing body dysmorphic disorder.

What would participation involve?

Participants may use a digital tool or app, attend study visits with the research team.

Who is it mainly for?

This study appears to be mainly for people with body dysmorphic disorder.

What should you check before joining?

Ask about whether participation can be remote and what device access is needed, whether there is a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

Your next step

Check the study details

Check the official source, then confirm these points with the research team.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateEstimated: September 2022
Recruitment status
Unknown
Enrollment listed in the registry
150
Sponsor
Lille Catholic University
Sponsor type
University
Study type
Behavioral
Intervention type
OTHER
Study phase
Not clearly listed
Locations
Not clearly listed
Age range
From 15 Years to 26 Years
Official registry ID
NCT04804800
Official title
Virtual Reality Place in the Management of Body Dysmorphia Disorders in Anorexia Nervosa : Comparison of the Recommended Management and Virtual Reality Care Programs With or Without Multisensory Remedy

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Study ID: NCT04804800. We help you review the study, but cannot decide medical eligibility.

Recruitment & locations

Status unknown

Locations not listed

Registry details
Registry conditions (original wording)

Anorexia Nervosa; Dysmorphophobia

In practice

For you

Participation may contribute to research. Personal benefit is not guaranteed.

Ask the research team to explain the activities, time commitment, and follow-up involved.

Confirm the location and whether remote participation is possible with the research team.

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is this study trying to understand?

This study is exploring psychotherapy or therapy for people with body dysmorphic disorder. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.

What is a behavioral study?

This appears to be a behavioral / psychological / psychosocial study involving Experimental group 1 : Virtual Reality, Experimental group 2 : Virtual Reality + Multi Sensorial Remediation. Phase is mainly useful to check for medication studies and some device studies.

Who might this study be for?

This study may concern people with body dysmorphic disorder; age range: From 15 Years to 26 Years. The criteria appear strict, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.

What would I likely need to do?

You may take part in sessions or exercises related to habits, thoughts, emotions, or behaviors.

Could this study affect my mood, habits, motivation, or stress?

Behavioral studies can involve habits, emotions, motivation, stress, sleep, or ways of thinking. Ask whether the intervention could affect your mood or stress, and who to contact if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.

What practical constraints should I expect?

The likely practical burden appears very high. Things to check include multiple visits or assessments. Ask the study team about duration, visits, possible compensation, data access, and what happens if you want to stop.

Who is behind this study?

This study is sponsored by Lille Catholic University, which appears to be a university. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.

Can I still join this study?

Current recruitment is not confirmed. Check the official registry or contact the research team before making plans to participate.

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