The Archives section offers access to past issues of the International Journal of Global Perspectives in Mental Health Nursing. Researchers, practitioners, and educators can refer to the archived articles for historical context and a deeper understanding of the evolution of mental health nursing practices over time.
Explore Past Issues
- Volume 1(Issue 1) JANUARY- JUNE 2025
Research Articles
The Prevalence of Restless Legs Syndrome and Its Effects on The General Population’s Quality of Sleep in Mangalore, India
Vol.1(1); Pages:1-7. Published on May-2025
Abstract
RLS represents a common neurological disorder which frequently recurs while people remain still during nighttime hours and induces an unstoppable urge to move their legs. The research evaluates Restless Leg Syndrome prevalence together with its relationship to sleep quality in Mangalore’s general population of India. Researchers administered a structured questionnaire which contained the standardized tools namely the International Restless Legs Syndrome Study Group (IRLSSG) criteria and the Pittsburgh Sleep Quality Index (PSQI) during a crosssectional study. The random sampling method included individuals from every age category and background. The preliminary study results show that RLS affects many people in the population but happens most frequently in individuals between middle age and elderly. Buildings a strong relationship exists between RLS symptoms and poor sleep quality which demonstrates the need for expanded medical care awareness and early treatment methods. The general population of Mangalore reports poor sleep quality as a result of Restless Leg Syndrome. The approach of public health through education and early recognition and treatment of RLS assists in enhancing sleep health and general well-being.
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Dialysis Patients’ Relief of Restless Leg Syndrome: A Way to Enhance Their Quality of Life Managing several documents
Vol.1(1); Pages:8-15. Published on May-2025
Abstract
Analysis shows that Restless Leg Syndrome (RLS) known as Willis-Ekbom Disease appears frequently yet remains unknown by medical professionals when dealing with chronic kidney disease (CKD) and dialysis patients because prevalence studies indicate between 15% to 45% cases. The symptoms of RLS include an uncontrollable need to move the legs which worsen when people rest and during nighttime periods thus resulting in severe disturbance of sleep patterns with fatigue throughout the day coupled with depression along with reduced quality of life (QoL).Scientific studies today demonstrate the value of combining medication-based approaches with non-medicine treatments in RLS management for this patient group. Medical treatment options that include dopaminergic agents together with gabapentin and opioids demonstrate moderate effectiveness but patients need to face the risks of adverse effects alongside drug tolerance development. The promise of managing RLS in individuals under dialysis treatment comes from low-risk non-pharmacological methods which include aerobic and stretching exercises and foot massage in combination with Kinesio taping and virtual-reality-assisted aerobic therapy and acupoint stimulation techniques. The available treatments demonstrate major positive effects which help patients with hemodialysis get better sleep and decrease their symptoms and improve their quality of life.Studies demonstrate that RLS symptoms become more severe because of anemia conditions and iron deficiencies in addition to when someone receives dialysis and experiences psychological stress. The treatment of patients with RLS should incorporate continuous monitoring coupled with sleep evaluations coupled with individualized behavioral changes together with standard medical care. New research shows that treating Restless Legs Syndrome requires multiple healthcare disciplines in dialysis programs to improve both patient health and prolonged treatment results.
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Global Strategies for Integrating Rare Disease Education into Healthcare Systems and Public Awareness Programs
Vol.1(1); Pages:16-24. Published on May-2025
Abstract
The European population exceeds 30 million with rare diseases which doctors along with the public frequently misunderstand due to deficient education about these conditions. Recent medical research achievements fail to create a cohesive education system for rare diseases since countries employ varying and inconsistent educational approaches. This paper shows there is an immediate necessity to establish worldwide coordination and develop an education plan which addresses rare diseases at every healthcare level along with public society. This document examines present shortcomings while featuring effective rare disease instruction models before proposing legislative-based methods for merging rare disease information throughout medical training programs and medical service development and population health awareness programming. The global improvement of diagnosis and care for rare disease patients and enhancement of their quality of life requires an integrated educational system that welcomes all levels of care and accessibility.
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Enhancing Emotional Hardiness: The Vital Need for Psychological Assistance at the Rare Disease Stage Identification in Children
Vol.1(1); Pages:25-32. Published on May-2025
Abstract
The identification of rare diseases among children creates an intense and important developmental phase for parents as well as caregivers. When families encounter a rare diseases diagnosis their lives turn upside down through the combination of unknowns and medical jargon as well as insufficient medical information. This leads them into an advanced medical process which creates major psychological consequences. The initial phase of diagnosis brings severe distress and grief and anxiety together with feelings of being alone that severely affect both caregiver health and their ability to provide care. The specific nature of this condition causes the psychological distress to escalate because diagnosis delays and fragmented care pathways along with limited peer support become significant issues. Studies demonstrate that giving psychological support during diagnosis helps parents handle their emotions better and become stronger at making decisions while improving their interactions with healthcare staff. Implementing psychological services at the beginning of rare disease treatment fosters family resilience and decreases chronic mental health effects while delivering superior results for patients and their caretakers. The following abstract examines all aspects of delivering prompt tailored psychological support to families who receive a rare disease diagnosis.
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Methodological Considerations for Conducting Online Focus Group Discussions on Sensitive Health Topics with Underserved Patient Populations
Vol.1(1); Pages:33-40. Published on May-2025
Abstract
Online focus group discussions (OFGDs) represent an important methodological approach in qualitative research that helps researchers study complex and sensitive health matters involving underserved communities. Virtual group discussions function as a safe platform for collecting detailed qualitative information from people who resist or cannot participate in typical one-on-one interviews because of privacy issues or distance barriers. This study highlights the application of asynchronous OFGDs in exploring sexual health care experiences among trans masculine (TM) adults in the United States, a population that remains largely underserved in health research and clinical care.Drawing from a case study involving four asynchronous OFGDs conducted from September 2015 to February 2016, the article delves into the rationale for adopting this digital method, outlines the methodological framework, and reflects on the practical considerations necessary for successful implementation. This research examined both challenging aspects and assisting elements concerning preventive sexual health care through HPV screening and cervical cancer testing especially for patients who receive self-administered and provideradministered swabs. This paper delivers significant findings about running digital focus groups for sensitive themes through its systematic research on recruitment methods while providing participant interaction strategies and moderator guidelines alongside ethical guidelines.
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