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Not yet recruitingNCT07253545IOBBATUpdated Nov 28, 2025

IOBBAT - Impact of Basic Body Awareness Therapy on Body Awareness

An interventional study of Basic Body Awareness Therapy and Lecture in Perception, Self, Body Awareness and Self-Assessment, sponsored by Johannes Kepler University of Linz. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-28.

Sponsored by Johannes Kepler University of Linz · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Body awareness (BA) is an essential factor for health and well-being. In 2021, the IOBA (Impact on Body Awareness) study was conducted at the Institute of Physical Medicine \& Rehabilitation at Kepler University Hospital (Clinical Trials NCT05004272). This study investigated the effects of massage and gymnastics on BA in healthy individuals. The protocol provides a solid foundation for further research projects on BA. The aim of the present study is to examine the immediate effects of a Basic Body Awareness Therapy (BBAT) session compared to a lecture (control group) on BA and well-being, and to explore correlations with BA.

In a randomized controlled study with 60 physiotherapy students in two groups (BBAT and control group) the use of the ABC questionnaire and further German questionnaires (Short questionnaire on self-perception of the body, self-rating mood scale - revised) concerning body awareness and well-being should analyse the following hypothesis: There is a difference in the change of BA between intervention (BBAT) and control group, Before interventions demographic data and further questionnaires concerning health conditions of the participants (e.g. Simple Physical Activity Questionnaire, Short Form Health Survey, Brief Symptom Inventory) are administered. Correlations between BA and the results of these tests will be investigated too. All these analyses can provide insights into the effects of BBAT on BA. The identification of patterns in BA among students can be used for future comparisons with patient cohorts.

02

Conditions studied

  • Perception, Self
  • Body Awareness
  • Self-Assessment

Keywords

  • Basic Body Awareness Therapy
  • Body awareness
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Students in the 5th semester of the Bachelor's degree program in physiotherapy at FH JOANNEUM in Graz
  • Signed informed consent for participation

Exclusion criteria

Exclusion Criteria:

  • Pregnancy
  • Current illnesses or injuries that represent a contraindication for participating in the BBAT session
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Basic Body Awareness Therapy

    Basic Body Awareness Therapy (BBAT) is a treatment method that uses the body and its movements as a foundation for improved health. It incorporates everyday movements, Western therapeutic techniques, and elements from Tai Chi to enhance balance, stability, and movement quality. The exercises are simple to perform and focus attention on postural control and stability, breathing, and mental presence. The goal is to strengthen the individual's health resources, thereby promoting autonomy, activity, and participation.

    Procedure: Basic Body Awareness Therapy

  • Placebo comparator
    Lecture

    The control group receives a 20-minute video-based lecture on medicinal herbs

    Other: Lecture

Interventions

  • ProcedureBasic Body Awareness Therapy

    Basic Body Awareness Therapy (BBAT) is a treatment method that uses the body and its movements as a foundation for improved health. It incorporates everyday movements, Western therapeutic techniques, and elements from Tai Chi to enhance balance, stability, and movement quality. The exercises are simple to perform and focus attention on postural control and stability, breathing, and mental presence. The goal is to strengthen the individual's health resources, thereby promoting autonomy, activity, and participation.

  • OtherLecture

    The control group receives a 20-minute video-based lecture on medicinal herbs

05

What researchers measure

Primary outcomes

  1. Awareness Body Chart Questionnaire

    Body charts to fill in with colours according to intensity of body awareness. In sum, 51 body regions to colour with 5 different colour pencils (orange = "I can perceive with much detail", yellow = "I can perceive distinctly", green = "I can perceive", blue = "I can perceive indistinctly", black = "I cannot perceive"). To quantify the information, every region of the body will be coded as an extra item and the data of the colours will be transcribed: orange (= 5), yellow (= 4), green (= 3), blue (= 2), black (= 1). Higher values mean higher intensity of body awareness. In the case of pain, the pain location can also be marked on the body chart with a red pen and recorded on a 100 mm Visual Analogue Scale from 0 (no pain) to 100 (unbearable pain).

    Time frame: Before intervention

  2. Awareness Body Chart Questionnaire

    Body charts to fill in with colours according to intensity of body awareness. In sum, 51 body regions to colour with 5 different colour pencils (orange = "I can perceive with much detail", yellow = "I can perceive distinctly", green = "I can perceive", blue = "I can perceive indistinctly", black = "I cannot perceive"). To quantify the information, every region of the body will be coded as an extra item and the data of the colours will be transcribed: orange (= 5), yellow (= 4), green (= 3), blue (= 2), black (= 1). Higher values mean higher intensity of body awareness. In the case of pain, the pain location can also be marked on the body chart with a red pen and recorded on a 100 mm Visual Analogue Scale from 0 (no pain) to 100 (unbearable pain).

    Time frame: Immediately after intervention

Secondary outcomes

  1. Short questionnaire on self-perception of the body

    Verbal questionnaire concerning body awareness. 20 items (5 = "I can perceive with much detail", 4 = "I can perceive distinctly", 3 = "I can perceive", 2 = "I can perceive indistinctly", 1 = "I cannot perceive"). Higher values mean higher intensity of body awareness.

    Time frame: Before intervention

  2. Short questionnaire on self-perception of the body

    Verbal questionnaire concerning body awareness. 20 items (5 = "I can perceive with much detail", 4 = "I can perceive distinctly", 3 = "I can perceive", 2 = "I can perceive indistinctly", 1 = "I cannot perceive"). Higher values mean higher intensity of body awareness.

    Time frame: Immediately after intervention

  3. Self-rating mood scale - revised

    Verbal questionnaire concerning mood status. 24 pairs of oppositional adjectives concerning mood: One of them or \<neither nor\> should be ticked, depending on how it best corresponds to the current situation. The negative pole = 2. The positive pole = 0. \<neither nor\> = 1. Higher sum scores indicate worse subjective mood, lower values better mood.

    Time frame: Before intervention

  4. Self-rating mood scale - revised

    Verbal questionnaire concerning mood status. 24 pairs of oppositional adjectives concerning mood: One of them or \<neither nor\> should be ticked, depending on how it best corresponds to the current situation. The negative pole = 2. The positive pole = 0. \<neither nor\> = 1. Higher sum scores indicate worse subjective mood, lower values better mood.

    Time frame: Immediately after intervention

Other outcomes

  1. Simple Physical Activity Questionnaire

    Questionnaire to survey physical activity: It should show a snapshot of hours per day of an average day in the past week. The time in bed, the time while doing sedentary work (including dozing), while walking, while exercising and during other physical activities (such as household chores) is interrogated. The test does not measure the intensity of physical activity, but rather sorts it into the groups walking, sport and other categories.

    Time frame: Before intervention

  2. Short Form Health Survey (SF-12)

    Questionnaire on health-related quality of life. It consists of twelve questions relating to the last four weeks and yields statements about eight different dimensions of subjective health: general health perception, physical health, physically-conditioned role function, physical pain, vitality, mental health, emotionally-related role function, social functionality. Different Likert-Scales are used. A physical sum scale and a psychological sum scale can be calculated. The polarity of four items must be reversed so that higher values in all items and total scales reflect a better state of health. Normative data are available.

    Time frame: Before intervention

  3. Brief Symptom Inventory (BSI)

    Questionnaire on the burden of symptoms. The BSI is also called the Brief Symptom Check List (BSCL), it is a short form of the SCL-90 (Derogatis, 1993). The BSI consists of 53 items (physical as well as psychological symptoms), which are assessed subjectively on a Likert scale in relation to the last seven days from 0 = "not at all" to 5 = "very strong". The items result in nine scales: somatization, obsession-compulsion, interpersonal sensitivity, depression, anxiety, hostility, phobic anxiety, paranoid ideation and psychoticism.

    Time frame: Before intervention

  4. Beck Depression Inventory II (BDI-II)

    The BDI-II represents a self-rating instrument to assess the severity of depression. Four statements are given for each of 21 questions, from which the one that best describes how the person has felt in the past week is to be selected. In scoring, each item is given a score of 0 to 3, depending on the choice (higher number means higher depression scores), and after directly adding the scores of the individual items, a total score of 0 to 63 is obtained.

    Time frame: Before intervention

  5. Insomnia Severity Index (ISI)

    The ISI is a self-assessment questionnaire used to evaluate the nature, severity, and impact of insomnia over the past two weeks. The ISI contains seven items rated with a five-point Likert scale (0 = not at all, 4 = very severe problem), with the total score ranging from 0 to 28. Higher scores indicate greater severity of insomnia. Scores from 0-7 are considered no insomnia, 8-14 is subthreshold insomnia, 15-21 is moderate insomnia, and 22-28 is severe insomnia.

    Time frame: Before intervention

  6. Body Mass Index

    Relation of body weight to the square of body height

    Time frame: Before intervention

  7. Like/Dislike Body Chart

    As an extension to the ABC, this questionnaire is intended to answer the question of whether there are areas of the body that one particularly likes about oneself or that one dislikes about oneself. If yes, one can draw these with a purple color pencil ("particularly like") and/or with a gray color pencil ("do not like") in an extra Body Chart.

    Time frame: Before intervention

  8. Additional questions

    Questions on demographic data and chronic complaints and current illnesses

    Time frame: Before intervention

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07253545
Lead sponsor
Johannes Kepler University of Linz
Collaborators
Medical University of Graz, FH Joanneum Gesellschaft mbH, Kepler University Hospital
Responsible party
Sponsor
First posted
Nov 28, 2025
Start date
Nov 2025 (estimated)
Primary completion
Nov 2025 (estimated)
Completion
Dec 2025 (estimated)
Last update
Nov 28, 2025

Study contacts

Ursula Danner, Dr.
Contact
ursula.danner@kepleruniklinikum.at
+43 (0)5 7680 87 27111
Christian Mittermaier, M.D.
study director · Kepler University Clinic, Dept. of Physical Medicine & Rehabilitation

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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