N/A
Completed N=39
A Physical Activity Program to Disrupt Sedentary Time in Older Latinos
Source: ClinicalTrials.gov NCT04507464 ↗Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Jul 2023
Primary outcomePrimary: Number of Sedentary Bouts — -11.58; -2.47 Sedentary bouts
Summary
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Sedentary Bouts |
-11.58; -2.47 | — |
| PRIMARY Time in Sedentary Bouts |
-347.7; -27.53 | — |
| SECONDARY Trail Making Test A |
.43; .31 | — |
| SECONDARY Trail Making Test B |
-35.26; 7.19 | — |
| SECONDARY Picture Vocabulary Test |
.20; .25 | — |
| SECONDARY List Sorting |
1.26; 5.53 | — |
| SECONDARY Picture Sequence |
4.26; 4.32 | — |
| SECONDARY Oral Reading Recognition Test |
6.89; 1 | — |
| SECONDARY Crystalized Cognition |
3.95; .95 | — |
| SECONDARY Auditory Verbal Learning |
.26; .47 | — |
| SECONDARY Text Message Motivation. |
8.7 | — |
| SECONDARY Enjoyment of the Text Messages. |
8.8 | — |
| SECONDARY Text Messages Helping Exercise. |
8.9 | — |
| SECONDARY Difficulty Understanding Text Messages |
0.9 | — |
| SECONDARY Enjoyment of the Program. |
9.4 | — |
| SECONDARY Difficulty With the FitBit. |
1.7 | — |
Eligibility Criteria
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
Data sourced from ClinicalTrials.gov (NCT04507464). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.