Journal of Scleroderma and Related Disorders

Scope & Guideline

Connecting the dots in scleroderma research for better patient outcomes.

Introduction

Welcome to the Journal of Scleroderma and Related Disorders information hub, where our guidelines provide a wealth of knowledge about the journal’s focus and academic contributions. This page includes an extensive look at the aims and scope of Journal of Scleroderma and Related Disorders, highlighting trending and emerging areas of study. We also examine declining topics to offer insight into academic interest shifts. Our curated list of highly cited topics and recent publications is part of our effort to guide scholars, using these guidelines to stay ahead in their research endeavors.
LanguageEnglish
ISSN2397-1983
PublisherSAGE PUBLICATIONS LTD
Support Open AccessNo
CountryItaly
TypeJournal
Convergefrom 2016 to 2024
AbbreviationJ SCLERODERMA RELAT / J. Scleroderma Relat. Disord.
Frequency3 issues/year
Time To First Decision-
Time To Acceptance-
Acceptance Rate-
Home Page-
Address1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND

Aims and Scopes

The Journal of Scleroderma and Related Disorders focuses on advancing the understanding and management of systemic sclerosis and related conditions. It serves as a platform for innovative research that spans a wide array of clinical, epidemiological, and therapeutic aspects of scleroderma.
  1. Clinical Research on Systemic Sclerosis:
    The journal prioritizes original clinical studies that investigate various manifestations of systemic sclerosis, including its impact on organs such as the lungs, heart, and gastrointestinal tract.
  2. Therapeutic Approaches and Innovations:
    Research articles often explore novel therapeutic strategies and treatment protocols, including the use of biologics, immunosuppressants, and emerging therapies tailored to scleroderma.
  3. Patient-Centered Care and Quality of Life:
    The journal emphasizes studies that assess the quality of life and patient-reported outcomes for individuals with systemic sclerosis, highlighting the importance of psychosocial factors in disease management.
  4. Epidemiological and Public Health Studies:
    There is a consistent focus on epidemiological research that addresses the prevalence, risk factors, and long-term outcomes associated with systemic sclerosis across diverse populations.
  5. Interdisciplinary Approaches:
    The journal encourages interdisciplinary research that brings together insights from various fields such as rheumatology, dermatology, cardiology, and nutrition to provide a holistic understanding of systemic sclerosis.
Recent publications in the Journal of Scleroderma and Related Disorders indicate several emerging themes that reflect the evolving landscape of research in systemic sclerosis. These trends highlight areas of growing interest and potential impact on clinical practice.
  1. Impact of COVID-19 on Systemic Sclerosis:
    An increasing number of studies address the implications of COVID-19 on the management and outcomes of patients with systemic sclerosis, emphasizing the need for adaptive care strategies during the pandemic.
  2. Nutrition and Lifestyle Interventions:
    There is a rising focus on the role of nutrition and lifestyle factors in the management of systemic sclerosis, exploring how these elements can influence disease progression and patient well-being.
  3. Digital Health and Telemedicine:
    Emerging research is examining the use of digital health technologies and telemedicine in the management of systemic sclerosis, particularly in enhancing patient access to care and improving monitoring.
  4. Mental Health and Psychosocial Factors:
    Studies increasingly explore the psychosocial dimensions of living with systemic sclerosis, including the effects of mental health on disease management and quality of life.
  5. Machine Learning and Diagnostic Innovations:
    There is a growing interest in the application of machine learning and other advanced technologies to improve the diagnosis and management of systemic sclerosis, reflecting broader trends in healthcare innovation.

Declining or Waning

While the Journal of Scleroderma and Related Disorders continues to expand its focus, certain themes appear to be declining in prominence. This trend may reflect shifts in research priorities or advancements in understanding that have influenced the scope of inquiry.
  1. Rare and Uncommon Manifestations:
    Research focusing on rare manifestations of systemic sclerosis, such as specific types of skin involvement or rare comorbidities, has decreased. This may indicate a shift towards more prevalent and impactful aspects of the disease.
  2. Historical Perspectives and Case Reports:
    There has been a noticeable reduction in the publication of historical case reports and vignettes, suggesting a possible move towards more data-driven, clinical, and experimental research.
  3. Basic Science Research:
    The journal has seen a waning interest in basic science studies that do not directly translate to clinical implications, possibly due to a growing emphasis on translational research that bridges bench to bedside.

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