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Brief Single-Session Body Neutrality Program for LGBTQ+ Adults in Central Alabama

2026년 5월 27일 업데이트: Tiffany Brown, Auburn University
LGBTQ+ individuals tend to have elevated risks for eating disorders (ED), possibly due to minority stress. For LGBTQ+ individuals living in rural Alabama, they tend to experience high levels of anti-LGBTQ+ structural stigma and limited access to LGBTQ+-specific resources, which engender compounded risk for ED development and reduced access to care. Brief digital single-session intervention that incorporates psychoeducation about minority stress and body neutrality may be efficacious in reducing ED risk and improve positive body image among LGBTQ+ adults in rural areas. Prior research from another lab developed a single-session intervention (Project Body Neutrality) among LGBTQ+ adolescents indicated immediate positive changes in body image constructs and psychological well-being. The present project evaluates and adapts Project Body Neutrality, specifically for LGBTQ+ adults in a rural high-stigma, low-resource region.

연구 개요

상태

아직 모집하지 않음

상세 설명

Eating disorders (EDs) kill one person in the United States every 52 minutes, cost over $65 billion annually ($966 million annually in Alabama (AL) alone), have numerous barriers to treatment access, and are notoriously difficult to treat. Thus, scalable interventions that can target high-risk groups prior to ED onset are critical to reducing both the public health burden and number of people suffering from EDs. Researchers have found that LGBTQ+ adults are at a significantly increased risk for EDs. Further, LGBTQ+ adults who live in rural areas with high levels of anti-LGBTQ+ structural stigma and limited access to LGBTQ+-specific resources may have compounded risk for ED development and reduced access to care. Despite this glaring inequity, few scalable programs exist to prevent EDs in LGBTQ+ populations. Thus, the present study proposes a pilot digital single-session intervention to reduce ED risk for LGBTQ+ adults in a high-stigma, low-resource region of AL.

LGBTQ+ people represent a high-risk group for EDs due to minority stressors. LGBTQ+ individuals have a 2-3 fold increased risk for developing an ED compared to their cisgender heterosexual peers. LGBTQ+ young adults also exhibit higher rates of overall ED symptoms, binge eating, dieting, vomiting, laxative, or diet pill use, muscle-building supplement use, and fasting compared to their non-LGBTQ+ peers. Researchers, using minority stress theory, have identified that increased risk is due, in part, to chronic stressors (e.g., prejudice, victimization, discrimination, internalized homophobia and/or transphobia, sexual identity concealment) due to being part of a marginalized group. These stressors are exacerbated for LGBTQ+ people of Color and those living in poverty. Additionally, LGBTQ+ individuals living in rural areas have increased vulnerability for mental health concerns and EDs. LGBTQ+ adults living in rural areas that have high prevalence of anti-LGBTQ+ structural stigma (e.g., discriminatory laws, policies, and community attitudes that promote unequal treatment) and low access to LGBTQ+-specific coping resources (e.g., LGBTQ+ centers, specialized healthcare) have increased risk for mental health problems compared to their urban peers. Further, individuals living in rural areas of AL, especially rural people of Color, often experience high degrees of medical mistrust due to lack of culturally competent care and history of medical abuse, which further increases disparities in broader health care access and utilization. Given the commonality of EDs in rural areas, high LGBTQ-stigma, and limited resources, LGBTQ+ adults living in rural regions of AL may represent a particularly vulnerable and underserved group for EDs.

Despite consistent research supporting increased ED risk among LGBTQ+ individuals, no ED prevention efforts have targeted minority stressors in rural LGBTQ+ adults, who need these interventions the most. Brief digital single-session intervention that incorporates psychoeducation about minority stress and body neutrality may be efficacious in reducing ED risk and improve positive body image among LGBTQ+ adults in rural areas. A recent randomized controlled trial developed a similar single-session intervention among LGBTQ+ adolescents (13-17 years old) in the United States. This Project Body Neutrality study indicated immediate positive changes in participants' body satisfaction, functionality appreciation, hopelessness, and perceived agency. This study supports the potential of online single-session intervention in addressing LGBTQ+ populations' eating pathology and body image concerns. Importantly, research suggests that the use of community-engaged research methodologies, where members of the community are actively engaged in research study design, development, and implementation, are critical for addressing the needs of minoritized communities and mitigating medical mistrust. Indeed, community-engaged research is a common approach to help reduce health disparities in diverse LGBTQ+ populations and our team has successfully adapted multi-session body image interventions for LGBTQ+ populations (e.g., the PRIDE Body Project) using a community-engaged approach in both rural and urban settings.

The present project evaluates and adapts Project Body Neutrality for LGBTQ+ adults in a rural high-stigma, low-resource region. The proposed study will recruit N = 40 LGBTQ+ adults in central AL to complete our program and pre-intervention and post-intervention assessments. The investigators hypothesize that this intervention program will effectively address LGBTQ+ adults' eating pathology, as well as their experience of minority stress, and improve their positive body image, especially their functionality appreciation.

연구 유형

중재적

등록 (추정된)

40

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Alabama
      • Auburn, Alabama, 미국, 36830
        • Auburn University
        • 연락하다:
        • 수석 연구원:
          • Tiffany A Brown, Ph.D.

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

예

설명

Inclusion Criteria:

  • At least 18 years old,
  • Identify as LGBTQ+,
  • Currently living in one of the following AL counties: Lee, Dallas, Lowndes, Autauga, Coosa, Elmore, Tallapoosa, Macon, or Russell
  • Have internet access (either via computer/tablet, mobile phone, or community center [e.g., library])

Exclusion Criteria:

  • Being less than 18 years old,
  • Identifying as cisgender and heterosexual,
  • Not living in central AL,
  • Not having internet access.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Single session body neutrality program
Single session body neutrality program is a brief, 30-minute digital intervention program. Participants will at first be given a brief introduction to body neutrality and minority stress. Then, they will be given fictional vignettes of based on common regional examples of body image stressors for LGBTQ+ individuals and practice giving advice to them. Finally, participants are provided with their customized body neutrality action plan based on their responses during the intervention program.
Single session body neutrality program is a brief, 30-minute digital intervention program. Participants will at first be given a brief introduction to body neutrality and minority stress. Then, they will be given fictional vignettes of based on common regional examples of body image stressors for LGBTQ+ individuals and practice giving advice to them. Finally, participants are provided with their customized body neutrality action plan based on their responses during the intervention program.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Functionality Appreciation Scale
기간: baseline and immediately after the intervention
Assesses changes in functionality appreciation (7 items, 7-point scale), with higher scores indicating higher levels of functionality appreciation.
baseline and immediately after the intervention
Body Image State Scale
기간: baseline and immediately after the intervention
Assesses changes in one's evaluative/affective body image states (6 items, 9-point scale), with higher scores indicating more favorable body image states.
baseline and immediately after the intervention
Positive and Negative Affect Schedule-Negative Affect
기간: baseline and immediately after the intervention
Assesses changes in one's negative affect (20 items, 5-point scale), with higher scores indicating higher levels of negative affect.
baseline and immediately after the intervention
Internalized stigma among LGBTQ+ people scale
기간: baseline and immediately after the intervention
Assesses changes in one's internalized LGBTQ+ stigma (5 items, 5-point scale), with higher scores indicating higher levels of internalized LGBTQ+ stigma.
baseline and immediately after the intervention

2차 결과 측정

결과 측정
측정값 설명
기간
Objectified Body Consciousness Scale- Surveillance scale
기간: baseline
Assesses the extent to which one monitors one's physical appearance (8 items, 7-point scale), with higher scores indicating higher levels of body monitoring.
baseline
Eating Disorder Examination Questionnaire-10 item, 3 factor
기간: baseline
Assesses the extent to which one endorses Dietary Restraint, Preoccupation and Eating Concern, and Shape/Weight Overvaluation (10 items, 7-point scale), with higher scores indicating higher levels of body monitoring.
baseline
Everyday Discrimination Scale
기간: baseline
Assesses the frequency one experience day-to-day discrimination (9 items, 6-point scale), with higher scores indicating higher frequency of everyday discrimination.
baseline

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 8월 2일

기본 완료 (추정된)

2028년 8월 2일

연구 완료 (추정된)

2028년 8월 2일

연구 등록 날짜

최초 제출

2026년 5월 21일

QC 기준을 충족하는 최초 제출

2026년 5월 27일

처음 게시됨 (실제)

2026년 6월 2일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 2일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 27일

마지막으로 확인됨

2026년 5월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 2222

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다