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Where is an emotion? Using body focus as a method of improving emotion regulation to inform suicide prevention initiatives

Where is an emotion? Using targeted visceroception as a method of improving emotion regulation in healthy participants to inform suicide prevention initiatives

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000324112
Enrollment
65
Registered
2019-03-04
Start date
2019-05-13
Completion date
2019-05-13
Last updated
2019-10-28

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

Conditions

None listed

Brief summary

The project will investigate whether the awareness of emotion (by a process of "visceroception" - sensing the viscera) as it manifests in the body is connected with the ability to manage it effectively (i.e. “emotion regulation”). The central focus of the project is a particular aspect of this manifestation: whether emotional feeling is physically localised. Further, it investigates whether an inhibitory process impedes awareness of localisation and whether it is possible to train people to identify it. The ultimate aim of the project is to assess whether there are grounds for thinking this training could be used in suicide prevention efforts. The primary hypothesis is: one of the visceroception groups will show significantly faster reaction times (RTs) to emotional stimuli compared with both of the other groups after baseline and there will be a greater change between baseline and follow-up. Each of the visceroception groups separately and combined will show significantly faster RTs than the control group.

Interventions

Visceroceptive awareness intervention. This involves directing attention to the physiological activity of a part of the body, where these parts differ across experimental groups. One group will focus attention on cardiac activity with another group focussing on gut activity in the lower abdomen. These groups undertake the intervention over an extended period of 8 weeks, 6 days per week, 20 minutes per day. Participants will be provided with written instructions online (developed by the Princip

Visceroceptive awareness intervention. This involves directing attention to the physiological activity of a part of the body, where these parts differ across experimental groups. One group will focus attention on cardiac activity with another group focussing on gut activity in the lower abdomen. These groups undertake the intervention over an extended period of 8 weeks, 6 days per week, 20 minutes per day. Participants will be provided with written instructions online (developed by the Principal Investigator) for how to approach this daily task. These instructions will include the body posture to adopt during each session, the focal point for the task (being either cardiac or gastrointestinal, not skeletal), ensuring the set up in the room is comfortable (e.g. comfortable temperature, comfortable and stable chair), and common pitfalls when undertaking meditation (e.g. mind wandering). When beginning the task, participants in the cardiac focus group will be cued with an image highlighting the chest area, with those in the gut focus group being cued by an image highlighting the lower abdomen. They will be instructed to focus within the body at these locations. Further, there will be opportunities for participants to ask questions face to face and/or over email. The intervention (and knowledge of group allocation) will be introduced during an initial laboratory visit, which will be reinforced by the online materials. The first meditation session takes place after the initial laboratory visit. The Principal Investigator (PI) has based the intervention on instructions provided in journal articles using visceroception, in combination with a meditation framework taken from a traditional Zen Buddhist practice (the PI has 20 years' experience of this framework with the Zen Centre, London). This framework will be used to fix the bodily posture (upright position, curved lower back, chest out, ears in line with the shoulders, eyes lowered, one hand gripping the other in the lap) and set the environmental conditions for each daily session (room temperature, medium level lighting, no noise or other distractions such as food, and ensuring a comfortable room temperature) as well as some guidance on what is meant by focussing attention on physiological activity (i.e. emphasising the difference between attending to bodily locations and thinking about those locations). The intervention will take place in the participants' own home, using their own computer to access an online guided task. The task includes responding to several questions about any changes in emotional experience throughout the study period. In terms of adherence, all participants will be logging in to a website to complete the daily task. Each log in is automatically recorded, including time spent and all activities within the session. This includes the responses to the questions indicated previously. In the event that participants do not log in for more than 2 consecutive days, they will be contacted by the researcher. Further, at the 4-week midpoint, the researcher will contact each participant to check for any issues or difficulties they may be experiencing. This will be a brief Skype conversation or, otherwise, an email exchange.

Sponsors

University of Otago Wellington
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

(a) BMI equal to or lower than 30; 32 for Maori/PI; (b) Currently enrolled on a full time medical or nursing degree/diploma or allied health degree/diploma OR already qualified and working as a doctor/nurse/allied health professional; (c) Regular levels of physical activity: at least 150 minutes of moderate-intensity aerobic physical activity throughout the week or least 75 minutes of vigorous-intensity aerobic physical activity or an equivalent combination of moderate- and vigorous-intensity activity (based on World Health Organisation guidelines); (d) Normal or corrected vision; (e) Normal or corrected hearing; (f) Right-handed; (g) Aged 18-35 years; (h) Availability for the entire study period.

Exclusion criteria

(a) Poor physical health (including gastrointestinal disorders, heart disease, kidney disease, respiratory disease, plus medication use that may influence awareness or creation of bodily sensations); (b) Poor psychological, psychiatric or neurological health (e.g. alexithymia, schizophrenia, depression, anxiety, brain injury); (c) Somatosensory amplification; (d) If female: in pregnancy; (e) Formal dance or drama training; (f) Formal musical training; (g) Formal meditation or mindfulness training.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026