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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06386055
Other study ID # STUDY00007545
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 15, 2024
Est. completion date December 1, 2024

Study information

Verified date October 2023
Source State University of New York at Buffalo
Contact Lina Mu, MD,PhD
Phone 7168295381
Email linamu@buffalo.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a small pilot intervention trial in which we will collect preliminary data to demonstrate the feasibility of an intervention study.


Description:

This is a pilot randomized, control, clinical trial. We will recruit 24 adults in Buffalo and randomize them to the physical intervention groups. The intervention group will be provided with physical activity courses. We will follow up all participants until the end of the study. We will collect their baseline information via questionnaire, and at the end of the follow-up we will collect the exit questionnaire and biospecimen. The study aims to demonstrate our ability to recruit eligible participants and provide data of the compliance of participants to the intervention.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date December 1, 2024
Est. primary completion date October 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 35 Years to 55 Years
Eligibility Inclusion Criteria: - 1) age 35-55 years old; 2) plan to stay in Buffalo most of the time in the next three months; 3) no adverse conditions Exclusion Criteria: - those with unstable or life-threatening medical conditions. The pilot study will also demonstrate our ability to recruit the modified study population.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Active exercise
The intervention group will be provided with training courses for 3 months.

Locations

Country Name City State
United States University at Buffalo Buffalo New York

Sponsors (1)

Lead Sponsor Collaborator
State University of New York at Buffalo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary blood pressure blood pressure will be measured 3 months
Secondary Self-report questionnaire This includes how participants feel about the intervention program 3 months
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