Implicit Attitudes Toward Body Shape Among Blind Women

Sponsor
University of Haifa (Other)
Overall Status
Completed
CT.gov ID
NCT05144906
Collaborator
(none)
64
1
6.4
9.9

Study Details

Study Description

Brief Summary

High levels of body image concerns and disordered eating in western women have been associated with the promotion of an unrealistically thin body ideal. The pressure to conform with the thin-ideal forms both explicit and implicit attitudes favoring thinness. Visual-based media depicting thin-idealized bodies plays a major role in forming such attitudes. However, attitudes favoring thinness can also be transmitted through non-visual communication such as peer pressure and significant others. The current study will examine if implicit attitudes favoring thinness and disliking overweight bodies can be formed without ever being exposed to visual-based media or being visually exposed to body shapes. To achieve this goal, the study will assess implicit attitudes towards thin and overweight bodies in congenitally blind women and those who were blinded early in life. The assessment will be carried out using a novel auditory weight-bias implicit association test.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Previous studies have demonstrated strong implicit associations between images portraying thin bodies and positive words and images portraying overweight bodies and negative words among healthy individuals in Western society. This so-called "implicit weight bias" is thought to represent individuals' unconscious or automatic stereotypical attitudes against being overweight. The goal of the current study is to examine implicit weight biases among congenitally blind as well as sighted women using a novel auditory version of the weight bias implicit association task. In this task, participants hear a series of words and are requested to classify each word using a motor response to the matching category. The categories used will be negative and positive words as well as words describing thin and overweight bodies. Implicit anti-fat bias is reflected by longer response times and higher error rates, when positive words and those describing overweight bodies require the same motor response and when negative words are coupled with words describing thin bodies compared to when positive and negative words are coupled with words describing thin and overweight bodies, respectively.

    The investigators have collected preliminary results in a sample of blind women (N = 18) in Israel. The investigators plan to a) expand the data collection in Israel to reach a sample of 30 blind women and to b) carry out a full replication of the study in an independent sample of blind and sighted women in the US. Data have not been collected yet for the US replication study. Based on the effect size of the the implicit bias effect (represented by the IAT D score) obtained in preliminary results in the Israeli sample (Cohen's D = 0.74), a power analysis using G*power was carried out and showed that a sample of 22 participants is sufficient to detect the IAT implicit bias effect with a power > 95% and an a-priori alpha set at 0.05.

    Based on preliminary results in the Israeli sample, it is hypothesized that:
    1. Blind women will demonstrate an implicit bias indicating preference for thin bodies and a dislike of overweight bodies. This effect will be reflected by slower response times when words describing thin bodies will be coupled with negative compared to positive words and when words describing overweight bodies will be coupled with positive compared to negative words. This implicit bias effect will be computed using the IAT's D algorithm.

    2. The implicit anti-fat bias effect (IAT D-score) will be comparable between sighted and blind women.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    64 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    Implicit Attitudes Toward Body Shape Among Blind Women: Evidence From an Auditory Implicit Association Test
    Actual Study Start Date :
    Dec 1, 2021
    Actual Primary Completion Date :
    Jun 15, 2022
    Actual Study Completion Date :
    Jun 15, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Blind women

    The blind women group will include women who are congenitally blind or that were blinded early in life (up to the age of 7).

    Sighted women

    Women with normal or corrected-to-normal eye sight.

    Outcome Measures

    Primary Outcome Measures

    1. Implicit Association Test [One assessment at baseline after study information and informed consent was given]

      IAT D-Score calculated for assessing an implicit weight bias. The IAT D score will be computed using the improved algorithm suggested by Greenwald et al. (2003). According to this algorithm, RTs longer than 10,000 ms will be deleted. Participants with more than 10% of the trials that are shorted than 300 ms will be excluded from the analysis. Mean RTs for correct trials will be computed for each block separately. Error trials will be replaced by the mean score of each block + 600 ms. Then, the difference in RTs between the practice stereotype incongruent and practice congruent conditions will be divided by their pooled SD. Then, the different in RTs between the test stereotype congruent and incongruent blocks will be divided by their pooled RTs. Lastly, the two scores form the practice and test blocks will be averaged to compute the IAT D score.

    Secondary Outcome Measures

    1. Sociocultural Attitudes Toward Appearance Questionnaire-4 (SATAQ-4R) [up to 72 hours after completion of the baseline assessment]

      The SATAQ-4R is a gender-specific self-report tool composed of 31 items in the female version. It includes four scales to evaluate the perceived pressure from family, peers, significant others, and the media to attain a thin body and three sub-scales that evaluate the desire to attain a lean body, to attain a muscular physique and overall concern with personal appearance. Participants rate their agreement with various statements on a 5-point scale.

    2. Ideal Body Stereotype Scale-Revised (IBSS-R) [up to 72 hours after completion of the baseline assessment]

      The IBSS-R measures the pursuit of the thin beauty ideal. Participants are asked to indicate to what extent they agree with six statements about what attractive women look like on a 5-point scale from strongly disagree to strongly agree. The total sum ranges from 0 to 30 with higher scores indicating a stronger internalization of the thin ideal.

    3. Body Parts Dissatisfaction Scale (BPDS) [up to 72 hours after completion of the baseline assessment]

      The BPDS assesses body dissatisfaction by asking the respondents to rate their satisfaction with 9 body parts on a scale from 1 (extremely dissatisfied) to 5 (extremely satisfied). Lower scores represent greater body dissatisfaction.

    4. Body mass index (BMI) [up to 72 hours after completion of the baseline assessment]

      Weight and height data will be collected via self-report in order to calculate BMI (kg/cm2).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes

    Blind Women

    Inclusion Criteria:
    • Aged 18-45 years.

    • Congenitally blind or blinded no later than the age of 7.

    • Inability to see themselves in the mirror.

    • Inability to recognize other people's faces or bodies.

    • Inability to use visual-based media.

    • Fluent English speakers.

    Exclusion Criteria:

    • Any condition that prevents the ability to use a computer.

    Sighted women

    Inclusion Criteria:
    • Aged 18-45 years old.

    • Corrected or corrected-to-normal vision.

    • Fluent English speakers.

    Exclusion Criteria:

    • Any condition that prevents the ability to use a computer.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Haifa Haifa Central Israel 3600100

    Sponsors and Collaborators

    • University of Haifa

    Investigators

    • Principal Investigator: Noam Weinbach, PhD, University of Haifa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Haifa
    ClinicalTrials.gov Identifier:
    NCT05144906
    Other Study ID Numbers:
    • 493-20
    First Posted:
    Dec 3, 2021
    Last Update Posted:
    Jul 6, 2022
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 6, 2022