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Mobility LimitationNCT05991076

Feasibility of a Community-based Dance Program for Latino Older Adults

An observational study of Mobility Limitation, run by University of Wisconsin, Madison at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of this study is to evaluate the feasibility and preliminary effectiveness of Activate Bailando, a 6-week community-based dance class offered in Spanish to older adults. Read more about this study

Who is it for?
Ages 55 years and older
Conditions the study is for
Mobility Limitation
What is being tested?
Latin Dance
How many people
18 participants
Where
1 siteUnited States
Study dates
8 Aug 2023to 3 Oct 2023
Phase
Observational
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 55 years and older
  • All sexes
  • Adult, Older adult

Study population: Community-dwelling older adults including Spanish-speaking older adults are enrolled in Activate Bailando, a community-based dance class.

Who may be able to join

  • Being over the age of 55
  • Willing and able to participate in the Activate Bailando class
  • Willing and able to complete data collection before and after the program

Who cannot join

  • Not Being over the age of 55
  • Not willing and able to participate in the Activate Bailando class
  • Not willing and able to complete data collection before and after the program

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Catholic Multicultural Center

    Madison, Wisconsin, 53713

Other trials in United States

About this study

Official title: Feasibility of Activate Bailando, a Community-based Dance Program, on Balance and Social Connectedness for Latino Older Adults

The objective of this study is to evaluate the feasibility and preliminary effectiveness of Activate Bailando, a 6-week community-based dance class offered in Spanish to older adults. 20 older adults in the Madison, Wisconsin area who are enrolled in Activate Bailando will complete a pre-and post-program test within 10 days for program start and completion.

Read the detailed description

The primary aim is to evaluate the feasibility of the Activate Bailando program based on measures of recruitment, retention, attendance, and acceptability.

The secondary aim is to evaluate the preliminary effectiveness of the program on metrics of balance, mobility, social connectedness, and fear of falling.

Being tested
Latin Dance
Keywords
Hispanic/Latinos, Older Adults
Medical subject headings
Mobility Limitation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Latin DanceOther

    The Activate Bailando class is a dance-focused exercise class that is offered once per week for one hour. The program has been developed by dance educators in the Madison area.

Study groups in NCT05991076
Study groupRoleWhat they receive
Activate Bailando Dance ProgramThe Activate Bailando program is a 6-week dance-focused exercise program that focuses on balance and social connectedness for community-dwelling Spanish-speaking older adults.
Receives: Other: Latin Dance

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Recruitment rate of participants who enroll in the study

    A proportion of participants enrolled in the class and those who participate in the data collection will be reported.

    Measured: Baseline

  2. Retention rate of participants who enroll and complete the study

    A proportion of participants who complete the pre data collection, attend at least half of the classes, and complete the post data collection.

    Measured: Baseline, posttest (up to 7 weeks)

  3. Attendance of Class Participation

    Participants will be asked how many classes they attended at the end of the program.

    Measured: Posttest (up to 7 weeks)

  4. Acceptability of participation in the class

    Participants will be asked what they enjoyed and what they thought could be improved from the class.

    Measured: Posttest (up to 7 weeks)

Secondary outcomes (5)
  1. Change in University of California Los Angeles (UCLA) Loneliness Scale

    A 3-item survey that measures three dimensions of loneliness: relational connectedness, social connectedness, and self-perceived isolation. The scale has three response categories: hardly ever, some of the time, often. The scores of each question are added to give a range of scores from 3 (least lonely) to 9 (most lonely).

    Measured: Baseline, Posttest (up to 7 weeks)

  2. Change in Timed Up and Go Results

    A mobility test records the time in seconds that it takes the participant to stand up, walk 10 feet (3 meters), walk back, and sit down again. An older adult who takes greater than or equal to 12 seconds to complete the task is at risk of falling.

    Measured: Baseline, Posttest (up to 7 weeks)

  3. Change in the 4-stage balance test

    A static balance test for 10 seconds in 4 different positions (stand feed side-by-side, place the instep of the foot so it is touching the big toes of the other foot, tandem stand, stand on one foot). The time the participant is able to balance in each position will be recorded in seconds. An older adult who cannot hold the tandem stand for at least 10 seconds is at increased risk of falling.

    Measured: Baseline, Posttest (up to 7 weeks)

  4. Changes in Falls Efficacy Scale (Short Version)

    A 7-item survey that measures confidence in one's own ability to complete daily activities without falling on a scale of 1-7 where lower scores indicate more extreme confidence.

    Measured: Baseline, Posttest (up to 7 weeks)

  5. Changes in Lubben Social Network Scale (LSNS-6)

    A 6-item scale that measures social engagement including family and friends. The total score is calculated by finding the sum of all items. For the LSNS-R, the score ranges between 0 and 60, with a higher score indicating more social engagement. For the LSNS-6, the score ranges between 0 and 30, with a higher score indicating more social engagement.

    Measured: Baseline, Posttest (up to 7 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Aug 2023
  2. Study start8 Aug 2023
  3. Primary completion3 Oct 2023
  4. Study completion3 Oct 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
18 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05991076
Sponsor's protocol ID
2023-0945
Other IDs
EDUC/KINESIOLOGY
Status last verified
Nov 2023
First submitted
4 Aug 2023
Last updated
14 Nov 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Mobility Limitation, run by University of Wisconsin, Madison at 1 site in United States.

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 3 inclusion and 3 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 14 Nov 2023. 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 United States. 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?

Recruitment rate of participants who enroll in the study (time frame: Baseline). The study lists 4 primary outcomes in all. 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 14 Nov 2023.

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