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Dancing for Better Aging: Evaluating the Impact of a Dance/Movement Therapy (D/MT) Program for Older Adults

Dancing for Better Aging: Evaluating the Impact of a Dance/Movement Therapy Program for Older Adults Through an Empirical Research Approach

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02455258
Enrollment
75
Registered
2015-05-27
Start date
2015-03-31
Completion date
2016-04-30
Last updated
2016-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging

Keywords

Inactivity

Brief summary

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.

Interventions

OTHERDance/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.

OTHERAerobics 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.

Sponsors

Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Z-score change on Cognitive Functioning0, 12 and 28 weeksAssessment of executive functions, processing speed and memory

Secondary

MeasureTime frameDescription
Z-score change on Dietary Screener Questionnaire0,12 and 28 weeks
Z-score change on Pittsburgh Sleep Quality Index (PSQI)0,12 and 28 weeks
Z-score change on Brief Pain Inventory0, 12 and 28 weeks
Z-score change on Psychological Condition0, 12 and 28 weeksSF-12
Z-score change on Physical Functioning0,12 and 28 weeksTimed up and go
Z-score change on Physical Condition0, 12 and 28 weeksVO2 peak
Z-score change on International Consultation on Incontinence Questionnaire-Urinary Incontinence ( ICIQ-UI)0, 12 and 28 weeksUrinary Incontinence

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026