- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02455258
Dancing for Better Aging: Evaluating the Impact of a Dance/Movement Therapy (D/MT) Program for Older Adults
July 26, 2016 updated by: Louis Bherer, Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
Dancing for Better Aging: Evaluating the Impact of a Dance/Movement Therapy Program for Older Adults Through an Empirical Research Approach
The aim of this study is to empirically evaluate the impact of a Dance/Movement Therapy program adapted to older adults.
Participants over 60 years old are enrolled in one of three groups: Dance/Movement Therapy, Aerobic Exercise or Waiting List (control group) for 12 weeks.
The training groups occur 3 times a week for 1 hour each session.
Physical condition, cognitive function, general health and lifestyle, and stress hormones are assessed at baseline, after 12 weeks and after 28 weeks.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
75
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
-
-
Quebec
-
Montreal, Quebec, Canada
- IUGM
-
-
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
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- aged 60 years and older
- sedentary or moderately sedentary (less than 150 minutes of moderate to vigorous exercise per week)
- have not participated in another similar study in the last year
- have not been exposed to a dance or dance/movement therapy program in the past year
- are not in a wheelchair
- have not had surgery in the past year
- have not smoked in the past 5 years
- do not consume more than 2 glasses a day of alcohol
- are not in treatment for major depression
Exclusion Criteria:
- progressive neurological disorder
- unstable medical conditions (unstable cardio illness in the past 6 months, cardiac or thyroid troubles or pituitary gland illness)
- contraindication for moderate physical activity (major orthopaedic limitations)
- suspicion of cognitive problems (score of 24 or less on the Mini-Mental State Examination)
- large uncorrected perceptual limits
- treatment of hormone therapy
- uncontrolled hearing loss
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Dance/Movement Therapy (DMT)
|
Each DMT session follows a similar structure of Opening, Warm up, Development, Cool Down and Closure.
Various themes dedicated to an aging population are addressed by the supervising dance/movement therapist through movement activities and using support material (i.e., props, music).
This group is provided in a group setting of maximum 10 participants at a time and occurs 3 times per week for 1 hour each session over the course of 12 weeks.
|
Active Comparator: Aerobics Exercise (AE)
|
The aerobics exercise program is composed of warm up exercises followed by cardiovascular training on a recumbent bicycle.
The intensity is set and progressively increased using each participants' individualized maximal aerobic power obtained in the baseline VO2 evaluation.
This program respects the recommendations made by the American College of Sports Medicine and their adaptations for aging populations.
Each session is supervised by a kinesiologist with 2 participants at a time.
The training occurs 3 times per week for 1 hour each session over the course of 12 weeks.
|
No Intervention: Waiting List
This group is placed on a waiting list and asked to refrain from making any changes to their current lifestyle.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Z-score change on Cognitive Functioning
Time Frame: 0, 12 and 28 weeks
|
Assessment of executive functions, processing speed and memory
|
0, 12 and 28 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Z-score change on Psychological Condition
Time Frame: 0, 12 and 28 weeks
|
SF-12
|
0, 12 and 28 weeks
|
Z-score change on Psychological Condition
Time Frame: 0, 12 and 28 weeks
|
Lubbens Social Network Scale
|
0, 12 and 28 weeks
|
Z-score change on Psychological Condition
Time Frame: 0, 12 and 28 weeks
|
Mental Health Continuum
|
0, 12 and 28 weeks
|
Z-score change on Psychological Condition
Time Frame: 0, 12 and 28 weeks
|
Health Promoting Lifestyle Profile
|
0, 12 and 28 weeks
|
Z-score change on Psychological Condition
Time Frame: 0, 12 and 28 weeks
|
State-Trait Anxiety Inventory
|
0, 12 and 28 weeks
|
Z-score change on Psychological Condition
Time Frame: 0, 12 and 28 weeks
|
Depression Scale
|
0, 12 and 28 weeks
|
Z-score change on Dietary Screener Questionnaire
Time Frame: 0,12 and 28 weeks
|
0,12 and 28 weeks
|
|
Z-score change on Pittsburgh Sleep Quality Index (PSQI)
Time Frame: 0,12 and 28 weeks
|
0,12 and 28 weeks
|
|
Z-score change on Brief Pain Inventory
Time Frame: 0, 12 and 28 weeks
|
0, 12 and 28 weeks
|
|
Z-score change on International Consultation on Incontinence Questionnaire-Urinary Incontinence ( ICIQ-UI)
Time Frame: 0, 12 and 28 weeks
|
Urinary Incontinence
|
0, 12 and 28 weeks
|
Z-score change on Physical Functioning
Time Frame: 0,12 and 28 weeks
|
Timed up and go
|
0,12 and 28 weeks
|
Z-score change on Physical Functioning
Time Frame: 0,12 and 28 weeks
|
10m walk
|
0,12 and 28 weeks
|
Z-score change on Physical Functioning
Time Frame: 0,12 and 28 weeks
|
Grip strength
|
0,12 and 28 weeks
|
Z-score change on Physical Condition
Time Frame: 0, 12 and 28 weeks
|
VO2 peak
|
0, 12 and 28 weeks
|
Z-score change on Physical Condition
Time Frame: 0, 12 and 28 weeks
|
Bone density scanning (DEXA)
|
0, 12 and 28 weeks
|
Z-score change on Physical Condition
Time Frame: 0, 12 and 28 weeks
|
BMI
|
0, 12 and 28 weeks
|
Z-score change on Physical Condition
Time Frame: 0, 12 and 28 weeks
|
Rockport walking aerobic fitness test
|
0, 12 and 28 weeks
|
Z-score change on Physical Condition
Time Frame: 0,12 and 28 weeks
|
Anthropometric measures composite
|
0,12 and 28 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
March 1, 2015
Primary Completion (Actual)
April 1, 2016
Study Completion (Actual)
April 1, 2016
Study Registration Dates
First Submitted
March 31, 2015
First Submitted That Met QC Criteria
May 26, 2015
First Posted (Estimate)
May 27, 2015
Study Record Updates
Last Update Posted (Estimate)
July 27, 2016
Last Update Submitted That Met QC Criteria
July 26, 2016
Last Verified
July 1, 2016
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CRIUGM
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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