- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05004272
IOBA - Impact on Body Awareness (IOBA)
December 10, 2021 updated by: Johannes Kepler University of Linz
Impact of Therapeutic Measures on Body Awareness
Due to social isolation and increased stress factors during the COVID-19 pandemic an increase of psychological and psychosomatic complaints in the population can be observed.
There is growing evidence of the importance of body awareness (BA) in these complaints.
The question arises how BA can be modified through therapeutic measures.
The Awareness Body Chart (ABC), an innovative non-verbal tool for investigating subjective body awareness, implemented in clinical practice brings to light astonishing findings of patients' bodily experiences which have not been collected through verbal communication so far.
In a randomized controlled study with 96 healthy adults in three groups (massage, gymnastics 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 hypotheses: Primary hypothesis: There is a difference in the change of BA between the massage group and the control group, and there is a difference in the change of BA between the gymnastics group and the control group.
Secondary hypothesis: There is a difference in the change of BA between the massage group and the gymnastics group.
Before interventions demographic data and further questionnaires concerning health conditions of the participants (Simple Physical Activity Questionnaire, Short Form Health Survey, Brief Symptom Inventory and additional questions) are administered.
Correlations between BA and the results of these tests will be investigated too.
All these analyses can provide innovative information about BA and be indicative in the use of physiotherapeutic measures.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
96
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Linz, Austria, 4020
- Kepler University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy volunteers
- Signing of informed consent by participants and head of the study
- Understanding of German language in order to be able to follow a lecture and complete questionnaires
Exclusion Criteria:
- Current sick leave
- Pregnancy
- Acute physical or psychological complaints on the day of study participation
- Chronic illnesses / disabilities which make it difficult to participate in a moderate exercise while standing
- Chronic diseases / impairments that make it difficult to lie prone for a massage
- Current illnesses or injuries that are a contraindication for hand massages or gymnastics
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Massage
|
20-minute manual full-body massage
|
|
Active Comparator: Gymnastics
|
20-minute moderate body workout
|
|
Placebo Comparator: Lecture
|
20-minute lecture on medicinal herbs
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Awareness Body Chart Questionnaire
Time Frame: Before intervention
|
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.
|
Before intervention
|
|
Awareness Body Chart Questionnaire
Time Frame: Immediately after intervention
|
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.
|
Immediately after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Short questionnaire on self-perception of the body
Time Frame: Before intervention
|
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.
|
Before intervention
|
|
Short questionnaire on self-perception of the body
Time Frame: Immediately after intervention
|
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.
|
Immediately after intervention
|
|
Self-rating mood scale - revised
Time Frame: Before intervention
|
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.
|
Before intervention
|
|
Self-rating mood scale - revised
Time Frame: Immediately after intervention
|
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.
|
Immediately after intervention
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Simple Physical Activity Questionnaire
Time Frame: Before intervention
|
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.
|
Before intervention
|
|
Short Form Health Survey (SF-12)
Time Frame: Before intervention
|
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.
|
Before intervention
|
|
Brief Symptom Inventory
Time Frame: Before intervention
|
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.
|
Before intervention
|
|
Body Mass Index
Time Frame: Before intervention
|
Relation of body weight to the square of body height
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Before intervention
|
|
Additional questions
Time Frame: Before intervention
|
Questions on demographic data and chronic complaints and current illnesses
|
Before intervention
|
|
Charlson Comorbidity Index
Time Frame: Before intervention
|
Questionnaire on comorbidities
|
Before intervention
|
|
Feedback form
Time Frame: Immediately after investigation
|
Personal feedback on questionnaires and measures
|
Immediately after investigation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 16, 2021
Primary Completion (Actual)
September 30, 2021
Study Completion (Actual)
September 30, 2021
Study Registration Dates
First Submitted
June 2, 2021
First Submitted That Met QC Criteria
August 5, 2021
First Posted (Actual)
August 13, 2021
Study Record Updates
Last Update Posted (Actual)
December 13, 2021
Last Update Submitted That Met QC Criteria
December 10, 2021
Last Verified
December 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- PMR_IOBA_01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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