Aging ProblemsNCT05015777
Effects of Jaques-Dalcroze Eurhythmics Program on Postural Stability in Elderly Women.
A study testing Emil Jaques-Dalcroze's Eurhythimcs Exercise Program in people with Aging Problems and Coordination Impairment, run by Poznan University of Physical Education at 1 site in Poland.
Trial summary
This study investigated the effect of exercise using the Emil Jaques-Dalcroze's method on the postural stability of women over 65 years of age. The study model was based on a randomized controlled trial - parallel group design. Read more about this study
- Who is it for?
- Ages 65 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Aging Problems, Coordination Impairment
- What is being tested?
- Emil Jaques-Dalcroze's Eurhythimcs Exercise Program
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 71 participants
- Where
- 1 sitePoland
- Study dates
- 6 Mar 2016to 20 Jun 2016
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- Women only
- Healthy volunteers accepted
- Older adult
Who may be able to join
- women,
- community-dwelling,
- had no contraindications to participation in physical activity,
- scored at least 8 on the Abbreviated Mental Ability Test .
Who cannot join
- taking medications that may interfere with natural control of postural stability,
- users of orthopaedic equipment,
- patients with neurological disease (Parkinson's or Alzheimer's),
- patients with significant visual and/or auditory perception impairment,
- subjects who undertake or have undertaken regular physical activity in the past three years
Trial locations and contacts
1 site in 1 country.
About this study
This study investigated the effect of exercise using the Emil Jaques-Dalcroze's method on the postural stability of women over 65 years of age. The study model was based on a randomized controlled trial - parallel group design.
Read the detailed description
Participants were recruited through advertisements in local newspapers and on the Internet, and covered the Poznań Metropolitan Area, Poland. Following randomization using the computer program Statistica 13.4 (TIBCO Software Inc., Palo Alto, CA)., the participants were divided into two groups: Intervention Group (IG) and Control Group (CG). The participants' postural stability was investigated by determining their ability to control the displacement of the body's center of pressure (COP). For this purpose, the Balance Platform model AccuSway Plus was used, together with the Balance Trainer software. The system recorded changes in COP position in the anteroposterior (AP) and mediolateral (ML) directions. The sampling rate was set at 100 Hz. The COP is a reliable parameter for evaluating postural stability and upright balance control. The results of the four COP parameters described below were statistically analysed.
- COP Path Length: sum of path lengths from the Subject Start Position to the intersection of the active target perimeter.
- COP Area Deviation: sum of areas where the COP path deviates from the straight line that intersects the Subject Start and End Positions.
- COP Total Time: time taken to complete the entire trial.
- COP Reaction Time: average reaction time to cross the perimeter of target, measured from the activation of the next target.
Two measurement sessions were held: the first (baseline) took place during the week before starting the exercise programme and the second (12-week follow-up) straight after its finish. Women with IG participated in the exercise programme, while women with CG were advised not to change anything about their current lifestyle, and in particular not to undertake any new structured physical activity. Those conducting the measurements were unaware of the purpose of this study and the fact that the participants were divided into groups.
Training programme. Training sessions took place twice a week for 45 minutes each over a period of 12 weeks. Each training included rhythmic exercises using the Jaques-Dalcroze Eurhythmics (JDE) method with piano accompaniment and electronically played music. Training sessions were conducted by a JDE specialist.
Balance Platform Test Participants had to perform a movement task while standing on a posturographic platform. A Feedback Balance Analysis protocol was used - the subjects saw a point on the screen that was a reflection of their COP. By tilting their body in different directions, they could observe changes in the position of their COP in real time. The participants' task was to do it in such a way as to direct their COP to the appropriate targets marked on the screen, in the right order.
Taking into account the natural heterogeneity of the group in terms of physical fitness due to the age of subjects, the distances of extreme areas in relation to the central area, and thus the range of deflection, were decided to be determined for each participant individually. For this purpose, first the maximum deflections of each subject in the AP and ML directions were determined, and then the software automatically determined the centres of targets at a distance of 75% of the maximum deflection in a given direction. This ensured that each subject leaned their torso relatively the same range and that the task was within their capabilities. The results of maximum torso lean ranges were also statistically analysed.
The test consisted of two main elements: 1) the COP point movement phase and 2) the COP point maintain phase. The task consisted of the COP point movement to individual targets (in a predetermined order), each time the COP point had to be maintained inside the area of each target for at least one second, after which the target became inactive (darker), which was a signal of its correct passing. At the same time, the next (active) target would light up, indicating that the COP point had to be moved to that target, where it again had to be held for a minimum of one second, and so on. Each time the extreme target was passed, it was necessary to return to the central target. A similar trial measuring changes in postural stability in a biofeedback model under the influence of training has already been used in other experiments.
The posturographic platform was fixed to a flat surface, in front of the subject at a distance of 1.5 meters at eye level was placed a 27 inch monitor. The room was soundproofed to ensure peace and quiet. On the platform there were lines specifying the proper distances and angles of feet placement in order to ensure that the subject stood in the same place during each subsequent trial. The feet on the platform were placed naturally, one next to the other at hip width, with the toes gently pointing outwards.
Each participant was given verbal instructions on how to perform the test, with particular emphasis on the fact that the test had to be carried out as quickly and accurately as possible, moving the COP point by the shortest possible route to the target, and once reached, trying to keep the COP point as still as possible in the centre of target until it became inactive (turned dark). The person conducting the test next performed a demonstration of the entire trial. The final step was for the subjects to perform two pre-test trials, followed by a third trial, the results of which were statistically analysed.
Statistical analysis The results of descriptive statistics were presented as means with standard deviation (mean±SD). Postural stability test results were presented as means and confidence intervals at the 95% level. A two-factor analysis of variance (ANOVA) was conducted. An eta square analysis was used to determine effect size. The post-hoc Tukey test was conducted in case of significant main or interaction effects. Differences between groups in the single study session area and between study sessions in the group area were determined using the Mann-Whitney U test with correction for continuity. Statistical significance level was set at 5%. All calculations were carried out using Statistica 13.4 (TIBCO Software Inc., Palo Alto, CA).
- Conditions
- Aging Problems, Coordination Impairment
- Being tested
- Emil Jaques-Dalcroze's Eurhythimcs Exercise Program
- Keywords
- postural stability, elderly, Dalcroze Eurhythmics, center of pressure, biofeedback
- Medical subject headings
- Ataxia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Emil Jaques-Dalcroze's Eurhythimcs Exercise ProgramOther
Training sessions took place twice a week for 45 minutes each over a period of 12 weeks. Each training included rhythmic exercises using the Jaques-Dalcroze Eurhythmics (JDE) method with piano accompaniment and electronically played music. Training sessions were conducted by a JDE specialist.
Exercises with the use of this method consist mainly in the repetition of preset musical sequences using body movements. In addition to the physical layer, the cognitive layer was equally important: while performing a given movement exercise, participants often had to focus in order to react appropriately to additional tasks, such as changes in sound pitch and rhythm of the piece.
| Study group | Role | What they receive |
|---|---|---|
| Intervention Group | Experimental | Participated in the exercise programme Receives: Other: Emil Jaques-Dalcroze's Eurhythimcs Exercise Program |
| Control Group | No intervention | Were advised not to change anything about their current lifestyle, and in particular not to undertake any new structured physical activity. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Ability to control the displacement of the body's center of pressure (COP).
Measured: 13 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Aug 2021
- Study start6 Mar 2016
- Primary completion20 Jun 2016
- Study completion20 Jun 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Aging ProblemsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- A study model based on randomized controlled trial - parallel group design was used.
- Masking
- Triple blind
- Who is masked
- Care provider, Investigator, Outcomes assessor
- Enrolment
- 71 participants (actual)
Sponsor and investigators
- Lead sponsor
- Poznan University of Physical Education
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- JAN ADAMCZYK, MA, Principal investigator, Poznan University of Physical Education
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05015777
- Sponsor's protocol ID
- 1/16
- Status last verified
- Aug 2021
- First submitted
- 9 Aug 2021
- Last updated
- 20 Aug 2021
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Aug 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Jaques-Dalcroze Eurhythmics Program on Postural Stability in Elderly Women.
- ClinicalTrials.gov ID
- NCT05015777
- Acronym / sponsor ID
- 1/16
- Conditions
- Aging Problems, Coordination Impairment
- Keywords
- postural stability, elderly, Dalcroze Eurhythmics, center of pressure, biofeedback
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 71 participants (actual)
- Lead sponsor
- Poznan University of Physical EducationUniversity, hospital or other
- Study start
- 6 Mar 2016 (actual)
- Primary completion
- 20 Jun 2016 (actual)
- Study completion
- 20 Jun 2016 (actual)
- First posted
- 20 Aug 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study investigated the effect of exercise using the Emil Jaques-Dalcroze's method on the postural stability of women over 65 years of age. The study model was based on a randomized controlled trial - parallel group design.
Detailed description
Participants were recruited through advertisements in local newspapers and on the Internet, and covered the Poznań Metropolitan Area, Poland. Following randomization using the computer program Statistica 13.4 (TIBCO Software Inc., Palo Alto, CA)., the participants were divided into two groups: Intervention Group (IG) and Control Group (CG). The participants' postural stability was investigated by determining their ability to control the displacement of the body's center of pressure (COP). For this purpose, the Balance Platform model AccuSway Plus was used, together with the Balance Trainer software. The system recorded changes in COP position in the anteroposterior (AP) and mediolateral (ML) directions. The sampling rate was set at 100 Hz. The COP is a reliable parameter for evaluating postural stability and upright balance control. The results of the four COP parameters described below were statistically analysed.
- COP Path Length: sum of path lengths from the Subject Start Position to the intersection of the active target perimeter.
- COP Area Deviation: sum of areas where the COP path deviates from the straight line that intersects the Subject Start and End Positions.
- COP Total Time: time taken to complete the entire trial.
- COP Reaction Time: average reaction time to cross the perimeter of target, measured from the activation of the next target.
Two measurement sessions were held: the first (baseline) took place during the week before starting the exercise programme and the second (12-week follow-up) straight after its finish. Women with IG participated in the exercise programme, while women with CG were advised not to change anything about their current lifestyle, and in particular not to undertake any new structured physical activity. Those conducting the measurements were unaware of the purpose of this study and the fact that the participants were divided into groups.
Training programme. Training sessions took place twice a week for 45 minutes each over a period of 12 weeks. Each training included rhythmic exercises using the Jaques-Dalcroze Eurhythmics (JDE) method with piano accompaniment and electronically played music. Training sessions were conducted by a JDE specialist.
Balance Platform Test Participants had to perform a movement task while standing on a posturographic platform. A Feedback Balance Analysis protocol was used - the subjects saw a point on the screen that was a reflection of their COP. By tilting their body in different directions, they could observe changes in the position of their COP in real time. The participants' task was to do it in such a way as to direct their COP to the appropriate targets marked on the screen, in the right order.
Taking into account the natural heterogeneity of the group in terms of physical fitness due to the age of subjects, the distances of extreme areas in relation to the central area, and thus the range of deflection, were decided to be determined for each participant individually. For this purpose, first the maximum deflections of each subject in the AP and ML directions were determined, and then the software automatically determined the centres of targets at a distance of 75% of the maximum deflection in a given direction. This ensured that each subject leaned their torso relatively the same range and that the task was within their capabilities. The results of maximum torso lean ranges were also statistically analysed.
The test consisted of two main elements: 1) the COP point movement phase and 2) the COP point maintain phase. The task consisted of the COP point movement to individual targets (in a predetermined order), each time the COP point had to be maintained inside the area of each target for at least one second, after which the target became inactive (darker), which was a signal of its correct passing. At the same time, the next (active) target would light up, indicating that the COP point had to be moved to that target, where it again had to be held for a minimum of one second, and so on. Each time the extreme target was passed, it was necessary to return to the central target. A similar trial measuring changes in postural stability in a biofeedback model under the influence of training has already been used in other experiments.
The posturographic platform was fixed to a flat surface, in front of the subject at a distance of 1.5 meters at eye level was placed a 27 inch monitor. The room was soundproofed to ensure peace and quiet. On the platform there were lines specifying the proper distances and angles of feet placement in order to ensure that the subject stood in the same place during each subsequent trial. The feet on the platform were placed naturally, one next to the other at hip width, with the toes gently pointing outwards.
Each participant was given verbal instructions on how to perform the test, with particular emphasis on the fact that the test had to be carried out as quickly and accurately as possible, moving the COP point by the shortest possible route to the target, and once reached, trying to keep the COP point as still as possible in the centre of target until it became inactive (turned dark). The person conducting the test next performed a demonstration of the entire trial. The final step was for the subjects to perform two pre-test trials, followed by a third trial, the results of which were statistically analysed.
Statistical analysis The results of descriptive statistics were presented as means with standard deviation (mean±SD). Postural stability test results were presented as means and confidence intervals at the 95% level. A two-factor analysis of variance (ANOVA) was conducted. An eta square analysis was used to determine effect size. The post-hoc Tukey test was conducted in case of significant main or interaction effects. Differences between groups in the single study session area and between study sessions in the group area were determined using the Mann-Whitney U test with correction for continuity. Statistical significance level was set at 5%. All calculations were carried out using Statistica 13.4 (TIBCO Software Inc., Palo Alto, CA).
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- A study model based on randomized controlled trial - parallel group design was used.
| Arm | Type | Receives |
|---|---|---|
| Intervention Group | Experimental | Other: Emil Jaques-Dalcroze's Eurhythimcs Exercise ProgramParticipated in the exercise programme |
| Control Group | No intervention | –Were advised not to change anything about their current lifestyle, and in particular not to undertake any new structured physical activity. |
Who may qualify
- Ages
- 65 years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Older adult
Key inclusion criteria (4 listed)
- women,
- community-dwelling,
- had no contraindications to participation in physical activity,
- scored at least 8 on the Abbreviated Mental Ability Test .
Key exclusion criteria (5 listed)
- taking medications that may interfere with natural control of postural stability,
- users of orthopaedic equipment,
- patients with neurological disease (Parkinson's or Alzheimer's),
- patients with significant visual and/or auditory perception impairment,
- subjects who undertake or have undertaken regular physical activity in the past three years
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Emil Jaques-Dalcroze's Eurhythimcs Exercise ProgramTraining sessions took place twice a week for 45 minutes each over a period of 12 weeks. Each training included rhythmic exercises using the Jaques-Dalcroze Eurhythmics (JDE) method with piano accompaniment and electronically played music. Training sessions were conducted by a JDE specialist. Exercises with the use of this method consist mainly in the repetition of preset musical sequences using body movements. In addition to the physical layer, the cognitive layer was equally important: while performing a given movement exercise, participants often had to focus in order to react appropriately to additional tasks, such as changes in sound pitch and rhythm of the piece. | Other | Intervention Group |
Primary outcome
Ability to control the displacement of the body's center of pressure (COP).
Time frame: 13 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Aug 2021.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
JAN ADAMCZYK, MA principal investigator
Poznan University of Physical Education
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Emil Jaques-Dalcroze's Eurhythimcs Exercise Program in people with Aging Problems and Coordination Impairment, run by Poznan University of Physical Education at 1 site in Poland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 20 Aug 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Ability to control the displacement of the body's center of pressure (COP). (time frame: 13 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2021.