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Weight Stigma in Women Who Are Obese: Assessing How an Acute Exposure to Stigma Negatively Impacts Cardiovascular Health

University of Connecticut logo

University of Connecticut

Status

Completed

Conditions

Obesity
Stigma, Social
Blood Pressure
Cardiovascular Disease Risk Factor

Treatments

Behavioral: Neutral video exposure
Behavioral: Stigma Video Exposure

Study type

Interventional

Funder types

Other

Identifiers

NCT04161638
H16-292HHC

Details and patient eligibility

About

The current study examined the influence of an acute weight stigma exposure on cardiovascular reactivity among women with obesity and high blood pressure and women with obesity and normal blood pressure.

Full description

The current study examined the influence of two video exposures, one containing scenes of weight stigma (STIGMA) and the other non-stigmatizing neutral (NEUTRAL) scenes, on cardiovascular reactivity as assessed by resting BP and ambulatory blood pressure (ABP) and heart rate (HR), among women with obesity and high BP (HBP) or normal BP (NBP). The investigators hypothesized that as a result of STIGMA compared to NEUTRAL, cardiovascular reactivity would be significantly greater immediately upon watching the video and persist outside of the laboratory over ambulatory conditions in women with obesity and HBP compared to women with obesity and NBP.

Enrollment

49 patients

Sex

Female

Ages

20 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Premenopausal
  • BMI > 30 kg/m2
  • No other known chronic cardiovascular or metabolic diseases besides hypertension

Exclusion criteria

  • Pregnant or planned on becoming pregnant
  • Took medications that may have affected the primary outcome of BP (e.g., stimulants for attention deficit hyperactivity disorder or steroids for asthma)
  • Currently using tobacco products
  • Diagnosed with an eating disorder

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

49 participants in 2 patient groups

High Blood Pressure
Experimental group
Description:
Ambulatory BP measurement was used to confirm the laboratory BP group classification according to the European Society of Hypertension. Participants were placed in the high blood pressure (HBP) group if they met any of the following criteria: 1) 19-hour average systolic BP/diastolic BP (SBP/DBP) \> 130/80 mmHg, 2) daytime (awake) average SBP/DBP \> 135/85 mmHg, or 3) nighttime (sleep) average SBP/DBP \> 120/70 mmHg.
Treatment:
Behavioral: Stigma Video Exposure
Behavioral: Neutral video exposure
Normal Blood Pressure
Experimental group
Description:
Participants were placed in the normal BP (NBP) group if they met all of the following criteria: 1) 19-hour average SBP/DBP \< 130/80 mmHg, 2) daytime (awake) average SBP/DBP \< 135/85 mmHg, and 3) night-time (asleep) average SBP/DBP \<120/70 mmHg.
Treatment:
Behavioral: Stigma Video Exposure
Behavioral: Neutral video exposure

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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