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Feasibility of a Yoga Intervention in Sedentary African-American Women

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Sedentary Behavior

Treatments

Behavioral: Yoga Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04710979
R34AT011036 (U.S. NIH Grant/Contract)
STUDY00010979

Details and patient eligibility

About

This study aims to test the feasibility, acceptability, safety of a 3-month hatha and restorative yoga intervention to decrease sedentary behavior, stress and blood pressure in sedentary African-American women.

Full description

This study aims to assess feasibility of a hatha and restorative yoga intervention compared to a control group. Investigators will examine feasibility of participant recruitment, retention and adherence; fidelity of intervention delivery; and intervention materials. Investigators also aim to evaluate the acceptability and safety of a hatha and restorative yoga intervention compared to a control group. Investigators will examine the acceptability of intervention location and strategies, class format, enjoyment of sessions, and safety of the intervention. Finally, investigators aim to test feasibility and appropriateness of the targeted outcomes for subsequent trials. Expected outcomes will be properly measured, but no comparisons between intervention and control groups will be made.

Enrollment

69 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Self-identified as an African-American woman at least 18 years old
  • Engaging in less than 30 minutes/week of moderate-to-vigorous physical activity
  • If employed, working in a sedentary occupation that requires primarily seated work; • If unemployed, typical day involves sedentary, primarily seated activities
  • Able to exercise for 20 minutes continuously
  • No pre-existing condition that limits physical activity
  • Access to a computer (or mobile device) and internet service

Exclusion criteria

  • Diagnosed with heart disease, diabetes, cancer, kidney, liver disease, major depression or bipolar disease
  • Take more than two daily medications for lipids or blood pressure
  • Current smoker

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

69 participants in 2 patient groups

Yoga Intervention Group
Experimental group
Treatment:
Behavioral: Yoga Intervention
Control Group
No Intervention group
Description:
Control participants will receive no guidance from the research staff to change their behavior.

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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