Air Pollution and Physical Activity: A Randomized Controlled Trial

Not Applicable

Not yet recruiting

• Conditions: Pollution; Exposure; Physical Inactivity
• Interventions: Behavioral: Active exercise

• Registration Number: NCT06386055
• Lead Sponsor: State University of New York at Buffalo

Brief Summary

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

Detailed 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.

Study Timeline

• Status Verified: 2023-10
• Study First Submitted: 2024-04-24
• Study First Submitted QC: 2024-04-24
• Last Update Submitted: 2024-04-24
• Study First Posted: 2024-04-26
• Last Update Posted: 2024-04-26
• Study Start: 2024-06-15
• Primary Completion: 2024-10-15
• Study Completion: 2024-12-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 24

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

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Intervention group 1	Active exercise	This is the physical intervention group 1(n=8).
Intervention group 2	Active exercise	This is the physical intervention group 2(n=8).

Primary Outcome Measures

Name	Time	Method
blood pressure	3 months	blood pressure will be measured

Secondary Outcome Measures

Name	Time	Method
Self-report questionnaire	3 months	This includes how participants feel about the intervention program

Trial Locations

Locations (1)

University at Buffalo; 🇺🇸 Buffalo, New York, United States