Skip to content

Hypnosis Induction and Height Experience in VR - Control Group Comparison and Three Sessions

Hypnosis Induction and Height Experience in Virtual Reality - Comparison With Control Group and Investigation of the Effect of Three Sessions

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06618456
Enrollment
101
Registered
2024-10-01
Start date
2024-05-07
Completion date
2024-10-31
Last updated
2024-10-01

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

Conditions

Acrophobia

Keywords

Virtual Reality, Hypnosis, Acrophobia, Exposition

Brief summary

This study attempts to test wether a VR-supported trance induction and a subsequent exposure to altitude in VR with hypnotic suggestions via Audio reduces acrophobia more than a control-group intervention without trance induction. Furthermore the study attempts to test if three sessions of the interventions within three weeks can lead to a stronger reduction of acrophobia than only one session. Participants will be selected via an online survey according to their score on the Height Interpersonal Questionnaire (HIQ). At the start of the study, participants will be screened by professional clinicians for any mental disorders. In the laboratory they will undergo one of the two interventions in VR (experimental group / control group) and complete questionnaires for three times within three weeks. On a separate day within these three weeks they will be placed in a 30-minute trance to test their suggestibility.

Detailed description

Prior to the measurement, those interested in the study will complete a screening questionnaire on acrophobia (HIQ) online. Besides they will be asked if they ever had negative experiences with VR or hypnosis. Only persons who do not report negative experiences with VR or hypnosis and who attain a HIQ score bigger than 29 will be invited to take part in the study. At the first appointment in the laboratory a screening with SCID questions about disorders that would lead to exclusion is conducted. On the basis of this second screening participants will be admitted to the study. Failure to meet the criteria (see eligibility section) will exclude participants from the study. At the start of the assessment session, participants will complete a sociodemographic questionnaire and again the HIQ. Participants are randomly assigned to one of the two groups. Based on group affiliation they either undergo a VR-supported trance induction or the same VR-program without the trance induction. Then there is an automatic transition to the altitude confrontation. Both groups receive the same VR altitude confrontation, the only difference is that in the experimental group a tree is presented near the participant whereas in the control group a parasol is presented at the same position. Thus the sentences that refer to the tree are changed in the audio of the control group. The height is increased to a maximum of 60 metres. Participants can stop the experiment at any time by pressing a button on a handheld joystick. During the confrontation, various events (e.g. rising balloons) generate additional altitude cues. The duration of the confrontation is approximately 15 minutes. Subsequently participants complete questionnaires about their fear of heights (HIQ) for a post-measurement of altitude anxiety and about their experience of presence (IPQ) and their experience of hypnotic depth (SSTT). Participants will undergo these questionnaires and the intervention three times within three weeks. On a separate day within these three weeks they will be placed in a 30-minute trance and given the Harvard Group Scale of Hypnotic Susceptibility (HGSHS) to test their suggestibility. The total time required for the participants ist therefore approximately three hours and 15 minutes.

Interventions

BEHAVIORALVR dive (with Hypnosis)

Participants experience a VR dive through a friendly underwater world. They get a trance induction via audio.

BEHAVIORALVR dive (without Hypnosis)

Participants experience a VR dive through a friendly underwater world. They are informed that this part of the VR is a familiarization phase to the VR and they do not get a trance induction.

BEHAVIORALHeight exposure

The participants go through a height exposure. They start at the ground level of a virtual city and move upwards in 3 meter steps until they reach a height of 60 meters. Participants focus on a yellow spot on a balcony in front of them, so that they can recognise the depth perimeter.

Sponsors

Milton Erickson Gesellschaft für klinische Hypnose
CollaboratorUNKNOWN
Milton Erickson Gesellschaft Stiftung
CollaboratorUNKNOWN
University Hospital Tuebingen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Participants are randomly assigned to one of the two groups (experimental group / control group). In the experimental group participants undergo a VR-supported trance induction. The participants in the control group are the same VR-environment but do not receive a trance induction. Then there is an automatic transition to the altitude confrontation (also in VR) in both groups. The experimental group receives hypnotic suggestions via audio, that partially refer to a tree positioned next to the participants in the VR-altitude-confrontation. In the control group this tree is replaced by a parasol in the VR and the text via audio. Besides from that they receive the same text as the experimental group.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* HIQ-Score \> 29 * informed consent

Exclusion criteria

* Negative previous experience with hypnosis * Negative previous experience with virtual reality * Mental illness (psychosis, post-traumatic stress disorder and/or personality disorder) * neurological disease * Acute or chronic disease (also anamnestic) that may affect brain metabolism: * pre-existing diabetes mellitus (E10-E14 according to ICD-10) * Renal insufficiency from stage 3 of the Kidney Disease Outcomes Quality Initiative * Uncontrolled hypertension (I10.x according to ICD-10) * Moderate or severe traumatic brain injury (GCS 3-12), or traumatic brain injury 2nd or 3rd degree with loss of consciousness of \> 30 minutes.

Design outcomes

Primary

MeasureTime frameDescription
Height intervention questionnaire (immediately before the intervention)Immediately (circa 1 minute) before the height exposure in all three sessionsMeasurement of acrophobia
Height intervention questionnaire (immediately after the intervention)Immediately (circa 1 minute) after the height exposure in all three sessionsMeasurement of acrophobia
Height intervention questionnaire (one-week-follow-up)One week after the third height exposureMeasurement of acrophobia
Height intervention questionnaire (three-months-follow-up)Three months after the third height exposureMeasurement of acrophobia
Subjective fear rating during height exposurealways 5 seconds after each rise in the height exposure in all three sessionsMeasurement of Fear on Likert scale (0 to 9)
Harvard Group Scale of Hypnotic Susceptibility (german brief form HGHSH-5)at a separate day within the three weeks, where the interventions take placeMeasurement of Suggestibility (minimum value = 0, maximum value = 5, higher scores imply higher suggestibility)

Secondary

MeasureTime frameDescription
Subjective Scale for Trance Depth(circa 5 minutes) after the height exposure in all three sessionsMeasurement of Trance Depth (minimum value = 38, maximum value = 152, higher scores imply higher subjective trance depth)
Igroup Presence Questionaire(circa 3 minutes) after the height exposure in all three sessionsSubjective Presence in the VR-experience (minimum value = -42, maximum value = +42, higher scores imply higher subjective presence)

Countries

Germany

Outcome results

None listed

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