IOBBAT - Impact of Basic Body Awareness Therapy on Body Awareness

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohannes Kepler University of Linz

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Students in the 5th semester of the Bachelor's degree program in physiotherapy at FH JOANNEUM in Graz

Signed informed consent for participation

Disqualifiers

Pregnancy

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Basic Body Awareness Therapy

    Procedure/Surgery

    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.

  • Lecture

    Other intervention

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

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Basic Body Awareness TherapyActive comparator 1 intervention
Group B: LecturePlacebo comparator 1 intervention

Trial outcomes

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

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Johannes Kepler University of Linz

Lead sponsor

Medical University of Graz

Collaborator

FH Joanneum Gesellschaft mbH

Collaborator

Kepler University Hospital

Collaborator

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