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Completed Not applicable Interventional Accepts healthy volunteers

Translation of an Evidence-Based Fall-Prevention Program Into Rural West Virginia Churches

ClinicalTrials.gov ID: NCT01961037

Public ClinicalTrials.gov record NCT01961037. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 10, 2026, 5:57 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Falls are the leading cause of death and injuries in adults over age 65 both nationally and in West Virginia. Rurality, age, physical inactivity, and chronic conditions, such as arthritis, are strong risk factors for falls in this population. West Virginia has a higher than average fall rate, the second oldest population, the greatest proportion of inactive adults, and the second highest prevalence of arthritis in the US. Thus, older adults in rural West Virginia are at high risk for falls and in great need of public health fall prevention programs. The Tai Chi: Moving for Better Balance (MFBB) program is a community-based, fall-prevention exercise program for older adults. A waiver of informed consent will be requested to conduct the telephone screenings to determine study eligibility. We will enroll up to 300 people in classes to be held at 20 churches in West Virginia. Classes will be held twice per week for 16 weeks and taught by certified MFBB instructors. Participants will be interviewed by telephone, have a brief physical function ability exam, and complete a questionnaire before starting the exercise class, at the end of the class, and 4 months later. The study is being conducted to answer the following questions: 1) What are the functional improvements of older adults who participate in a 16-week MFBB program; 2) What is the rate of falls for those adults; 3) What is the rate and severity of those fall-related injuries of the MFBB participants? The purpose of the study is to: 1) implement a 16-week intervention of MFBB with a 16-week follow-up, in older adults in churches in rural West Virginia; 2) describe functional and fall/injury outcomes. Ultimately, we will translate an efficacious and effective fall-prevention intervention into a new setting.

Study identification

NCT ID
NCT01961037
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
West Virginia University
Other
Enrollment
236 participants

Conditions and interventions

Interventions

Other

Eligibility (public fields only)

Age range
55 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2014
Primary completion
Feb 28, 2015
Completion
Feb 28, 2015
Last update posted
Dec 23, 2015

2014 – 2015

United States locations

U.S. sites
9
U.S. states
1
U.S. cities
7
Facility City State ZIP Site status
Hughes River Presbyterian Church Cairo West Virginia 26337
Wesley United Methodist Church Ellenboro West Virginia 26346
Harper Memorial Church Gandeeville West Virginia 25243
First Baptist Church Grantsville West Virginia 26147
First Assembly of God Harrisville West Virginia 26362
Cisco Community Church Petroleum West Virginia 26161
First Baptist Church Spencer West Virginia 25276
Memorial United Methodist Church Spencer West Virginia 25276
Spencer Presbyterian Church Spencer West Virginia 25276

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01961037, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 23, 2015 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01961037 live on ClinicalTrials.gov.

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