- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04507464
A Physical Activity Program to Disrupt Sedentary Time in Older Latinos (PAIS)
June 30, 2023 updated by: Ulf G. Bronas, University of Illinois at Chicago
To test the feasibility of an intervention designed to replace sedentary time with physical activity in older Latinos, delivered in their homes to improve cognitive function and brain connectivity.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
After being informed of the study and potential risks, all patients giving informed consent will undergo a focused phone interviews, followed by screening to determine eligibility.
Participants that meet inclusion criteria will undergo baseline cognitive function testing via video (following NIH toolbox guidelines for remote cognitive function assessment), followed by a one week measurement of sedentary time using a physical activity monitor (actigraphy).
At week 0, participants will be randomized into either a physical activity group to break up sedentary time or activity guidelines only in a 1:1 ratio.
Follow up occurs at 6 weeks using the same measures as baseline.
Study Type
Interventional
Enrollment (Actual)
39
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
-
-
Illinois
-
Chicago, Illinois, United States, 60608
- University of Illinois at Chicago
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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
55 years to 89 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- no history of major head trauma
- ownership of a smartphone
- ability to make video calls
Exclusion Criteria:
- Requires assistive ambulation;
- Unstable angina,
- Claudication
- severe arthritis,
- extreme dyspnea on exertion,
- Class III-IV heart failure;
- Current uncontrolled sustained arrhythmias,
- severe/symptomatic aortic or mitral stenosis,
- hypertrophic obstructive cardiomyopathy,
- severe pulmonary hypertension,
- active myocarditis/pericarditis,
- thrombophlebitis,
- recent systemic/pulmonary embolus (within 3 months);
- Revascularization procedures within the previous 6 months;
- Pregnancy
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Ecological Momentary Intervention
Participants will receive real time physical activity notifications via a wearable activity tracker and smartphone application.
|
Participants will wear a Fitbit that has been programmed to deliver a notification (a buzz) when activity has ceased for more than 10 minutes.
They will receive suggestions on their Illumivu mEMA smartphone app on how to replace sitting time with PA such as standing up 5 times or taking 20 steps, or even performing a short (20 seconds) preferred dance routine.
Fitbit data will be captured in real-time via the iCardia platform.
Participants will receive reminders from their smartphones to enter real-time feedback on activity options selected and how successful they were in adopting the option.
These data will allow tracking of underlying preferences for behaviors and to tailor the program accordingly.
Other Names:
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No Intervention: Physical Activity Guidelines
Participants will be sent general guidelines for disruption of sedentary time.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Sedentary Bouts
Time Frame: Baseline, 6 weeks
|
Change in number of bouts of sedentary activity at 6 weeks from baseline. One sedentary bout is defined as a 10 minute bout or longer where the activity count is less than 99 counts per minute. Sedentary Bout Parameters Minimum Length: 10 Minutes Minimum Count Value: 0 Counts Per Minute Maximum Count Value: 99 Counts Per Minute |
Baseline, 6 weeks
|
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Time in Sedentary Bouts
Time Frame: Baseline, 6 weeks
|
Change from baseline to 6 weeks in minutes spent in sedentary bouts
|
Baseline, 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trail Making Test A
Time Frame: Baseline, 6 weeks
|
Measure of pschycomotor speed.
Subjects connect a series of encircled numbers in numerical order.
The score is the time in seconds it takes the subject to complete the test.
A lower score/time is better.
Outcome is change in time to completion of TMT-A in seconds from baseline to 6 weeks.
|
Baseline, 6 weeks
|
|
Trail Making Test B
Time Frame: baseline, 6 weeks
|
Measure of executive function.
Subjects connect encircled numbers and letters in numerical and alphabetical order, alternating between the numbers and letters.
Score is the time in seconds it takes the subject to complete the test.
A lower score/time is better.
Outcome is change from baseline to 6 weeks in seconds.
Lower time is better.
|
baseline, 6 weeks
|
|
Picture Vocabulary Test
Time Frame: Baseline, 6 weeks
|
A measure of general vocabulary knowledge and is considered to be a strong measure of crystallized abilities (those abilities that are more dependent upon past learning experiences and are relatively consistent across the adult life span).
The respondent is presented with an audio recording of a word and four photographic images on the iPad screen, and is asked to select the picture that most closely matches the meaning of the word.
This is repeated over 4 minutes.
A theta score is very similar to a z-score, which is a statistic with a mean of zero and a standard deviation of one.
A higher score is better
|
Baseline, 6 weeks
|
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List Sorting
Time Frame: Baseline, 6 weeks
|
The List Sorting test requires immediate recall and sequencing of different visually and orally presented stimuli (i.e., "working memory").
Pictures of different foods and animals are displayed with accompanying audio recording and written text (e.g., "elephant"), and the participant is asked to say the items back in size order from smallest to largest, first within a single dimension (either animals or foods, called 1-List) and then on two dimensions (foods, then animals, called 2-List).
List Sorting is scored by summing the total number of items correctly recalled and sequenced on 1-List and 2-List, which can range from 0-26.
Higher scores indicate higher levels of working memory.
Change from baseline to post-test follow-up at 6-weeks is reported.
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Baseline, 6 weeks
|
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Picture Sequence
Time Frame: Baseline, 6 weeks
|
A measure developed for the assessment of episodic memory.
Participants are asked to recall the sequence of pictures demonstrated over two learning trials; sequence length varies from 6-18 pictures.
Participants are given credit for each adjacent pair of pictures they correctly placed.
The number of adjacent pairs placed correctly for each of trials 1 and 2 is converted to a theta score and a standard score is generated.
Change from baseline to 6 weeks is reported.
This provides a gauge of improvement or decline from one assessment to another, irrespective of demographic factors.
A change in a participant's Uncorrected Standard score (or theta score) from Time 1 to Time 2 represents an absolute change in the level of performance for that individual since the previous assessment.
Higher score is better.
|
Baseline, 6 weeks
|
|
Oral Reading Recognition Test
Time Frame: Baseline, 6 weeks
|
Participant is asked to read and pronounce letters and words as accurately as possible.
Administrator scores them as right or wrong (number correct words is used).
This test is a measure of reading decoding skill.
The Reading Test is a measure of reading decoding skill and, like vocabulary, is considered among the crystallized abilities; those abilities are generally more dependent upon past learning experiences and consistent across the adult life span.
Change in Reading Uncorrected score is reported and is useful in evaluating pure change in performance from one assessment to another.
Higher change in Uncorrected score for Reading would mean that the participant is able to correctly identify more difficult words on the subsequent assessment, which may indicate developmental growth or a return to a previous higher level of functioning.Change from baseline to 6 weeks is reported.
A higher score is better.
|
Baseline, 6 weeks
|
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Crystalized Cognition
Time Frame: Baseline, 6 weeks
|
This composite includes the Picture Vocabulary and Reading Tests and represent an accumulated store of verbal knowledge and skills.
The composite score is derived by averaging the standard scores of each of these measures, and then deriving standard scores based on this new distribution.
Uncorrected standard score is generated and reported.
Crystallized Cognition Composite score is considered a global assessment of individual verbal cognition.
Crystallized abilities are presumed to be more dependent on experience and less on biological influences.
They represent an accumulated store of verbal knowledge and skills.
Higher scores indicate higher levels of functioning.
Change in uncorrected standard score from baseline to 6 weeks is reported.
Higher change scores indicate improved levels of functioning
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Baseline, 6 weeks
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Auditory Verbal Learning
Time Frame: Baseline, 6 weeks
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The Rey auditory verbal learning task is a word-list learning task in which 15 unrelated words are presented orally (via audio recording) over three consecutive learning trials1.
After each presentation, the participant is asked to recall as many of the words as he/she can.
The Rey is scored by taking the sum of the number of words recalled across all trials (possible range is 0-45 words).
The raw score is most commonly used for interpretation of the Rey test, with higher scores representing better episodic memory.
Change from baseline to post-test follow-up at 6-weeks is reported.
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Baseline, 6 weeks
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Text Message Motivation.
Time Frame: 6 weeks.
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Participant reported rating on a scale from 0-10, with 0 being no motivation and 10 being the highest motivation provided by the ecological momentary intervention text messages.
Assessed at 6 weeks in the intervention group only.
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6 weeks.
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Enjoyment of the Text Messages.
Time Frame: 6 weeks.
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Participant reported rating on a scale from 0-10, with 0 being none and 10 being the highest, reported enjoyment of the ecological momentary intervention text messages.
Assessed at 6 weeks.
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6 weeks.
|
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Text Messages Helping Exercise.
Time Frame: 6 weeks.
|
Participants reported rating, on a scale from 0-10 with 0 being none and 10 being the highest, of the ecological momentary intervention text messages helping them to exercise.
Assessed at 6 weeks only
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6 weeks.
|
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Difficulty Understanding Text Messages
Time Frame: 6 weeks
|
Participants reported rating, on a scale from 0-10 with 0 being none and 10 being the highest, of the ecological momentary intervention text messages being difficult to understand.
Assessed at 6 weeks.
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6 weeks
|
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Enjoyment of the Program.
Time Frame: 6 weeks.
|
Participants reported rating, on a scale from 0-10 with 0 being none and 10 being the highest, of the enjoyment of the ecological momentary intervention.
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6 weeks.
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Difficulty With the FitBit.
Time Frame: 6 weeks.
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Participants reported rating, on a scale from 0-10 with 0 being none and 10 being the highest, of difficulty using the FitBit.
Assessed at 6 weeks.
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6 weeks.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Ulf G Bronas, PhD, University of Illinois at Chicago
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)
November 2, 2020
Primary Completion (Actual)
April 2, 2022
Study Completion (Actual)
April 2, 2022
Study Registration Dates
First Submitted
August 6, 2020
First Submitted That Met QC Criteria
August 7, 2020
First Posted (Actual)
August 11, 2020
Study Record Updates
Last Update Posted (Actual)
July 25, 2023
Last Update Submitted That Met QC Criteria
June 30, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-0739
- 2P30AG022849-16 (U.S. NIH Grant/Contract)
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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