Qualitative Software Research Articles

Barriers Pediatric PCP's Identify To Providing Gender-Affirming Care For Adolescents

PurposeBoth affirming environments and access to gender-affirming medical care have a positive impact on the mental health of transgender and gender diverse (TGD) youth, however, many TGD youth experience barriers in accessing this care. Pediatric primary care providers (PCPs) can play an important role in expanding access to gender-affirming care for TGD youth; however, few currently provide this care. The purpose of this study was to explore pediatric PCPs' perspectives regarding barriers they experience to providing gender-affirming care in the primary care setting. MethodsPediatric PCPs who had sought out support from the Seattle Children's Gender Clinic were recruited via email to participate in semistructured, one-hour Zoom interviews. All interviews were transcribed and then subsequently analyzed in Dedoose qualitative analysis software using a reflexive thematic analysis framework. ResultsProvider participants (n = 15) represented a wide range of experiences with respect to years in practice, number of TGD youth seen, and practice location (urban, rural, suburban). PCPs identified both health system and community-level barriers to providing gender-affirming care to TGD youth. Health system-level barriers included: (1) lack of foundational knowledge and skills, (2) limited clinical decision-making support, and (3) health system design limitations. Community-level barriers included (1) community and institutional biases, (2) provider attitudes regarding gender-affirming care provision, and (3) challenges identifying community resources to support TGD youth. DiscussionA multitude of health system and community-level barriers must be overcome in the pediatric primary care setting to ensure that TGD youth receive timely, effective, and more equitable gender-affirming care.

Towards Abstraction-based Probabilistic Program Analysis

Probabilistic programs that can represent both probabilistic and non-deterministic choices are useful for creating reliability models of complex safety-critical systems that interact with humans or external systems. Such models are often quite complex, so their analysis can be hindered by state-space explosion. One common approach to deal with this problem is the application of abstraction techniques. We present improvements for an abstraction-refinement scheme for the analysis of probabilistic programs, aiming to improve the scalability of the scheme by adapting modern techniques from qualitative software model checking, and make the analysis result more reliable using better convergence checks. We implemented and evaluated the improvements in our Theta model checking framework.

The emotional experience of treatment for locally advanced cervical cancer: Qualitative research findings from Brazil, China, Germany and the US.

e24217 Background: Little has been reported on the emotional journey of women treated for locally advanced cervical cancer (LACC). This study aimed to understand the expectations and experience of these women. Methods: Semi-structured telephone interviews were conducted in 2022 among women diagnosed with LACC in the past 2 years in Brazil (BR), China (CH), Germany (DE) and the US. This research elicited voices representing diverse demographic & socioeconomic groups. Trained moderators asked questions about experience and emotions during the journey from diagnosis through treatment. Transcripts were coded using NVivo qualitative analysis software to identify key themes that emerged from the data. Results: Ninety-two women in the US (n = 26), BR (n = 25), CH (n = 25), and DE (n = 16) participated, with mean age ranging from 35.7 years in BR to 53.4 years in DE. At the time of treatment decision, women reported receiving information about what to expect during treatment, including information about short and long term side effects of treatment (US 13/21, BR 14/22, CH 6/21, DE 6/9). Several women reported their doctor raising the chance to be cured after surgery/treatment (US 3/21, BR 12/22, CH 3/21, DE 1/9) and many women asked about prognosis (US 1/5, BR 2/6, CH9/17, DE 2/6). While most women reported that their doctors answered their questions and came away with positive feelings, some came away with negative feelings, did not ask questions generally (10/54) about diagnosis (7/37) and/or treatment (5/18) and blamed themselves (US 1/1, BR 1/2, CH2/3, DE 1/4). “No, I didn’t [believe all my questions were answered], but I believed the problem was about myself. At that moment, I had no idea what questions I should ask my doctor.” CN06 “No. As I was alone, I was so scared that I did not ask much.” BR25 Women shared that positive parts of their cancer journey were (a) gratitude and personal growth, (b) receiving support or making connections, (c) appreciation for their HCPs. Women noted negative aspects including (a) dealing with cancer or side effects, (b) facing death, recurrence or knowing others who have died, (c) encountering negative or unsupportive reactions from others. At the time of interview, most women (n = 68/92) described their general health as good, even while some continued experiencing minor symptoms or treatment side effects. Negative impacts of LACC included feelings of denial, worry, depression, fear, and worsening health. Conclusions: Currently, women report both positive and negative aspects of their LACC treatment decision and cancer care journey. A better understanding of women’s feelings when deciding on treatment, including feelings about how information needs are addressed, can promote a more positive interaction with the healthcare system, satisfaction with LACC treatment, experience living with the impact of the treatment they chose, and outlook for the future.

Sexual healthcare and at-home STI test collection: attitudes and preferences of transgender women in the Southeastern United States.

HIV and sexually transmitted infections (STIs) disproportionally affect transgender women in the United States, particularly in the Southeast where rates of HIV and bacterial STIs are especially high. Despite the high HIV/STI burden among transgender women, their engagement in sexual healthcare services, including HIV/STI testing, is low. Understanding reasons for this disconnect is essential in developing HIV/STI prevention efforts for this population, especially in the Southeastern US, where access to affirming sexual healthcare providers and resources is limited. We aimed to perform an exploratory qualitative study to describe the attitudes and preferences of transgender women living in Alabama with regards to sexual healthcare and at-home STI test collection. Transgender women ≥18 years old residing in Alabama were invited to participate in virtual individual in-depth interviews via Zoom. The interview guide explored participant experiences engaging with sexual healthcare services as well as preferences related to extragenital (i.e., rectal, pharyngeal) and at-home STI testing for gonorrhea and chlamydia. A trained qualitative researcher coded transcripts after each interview and iteratively amended the interview guide as themes emerged. Data were coded and thematically analyzed using NVivo qualitative software. Between June 2021-April 2022, 22 transgender women were screened and 14 eligible women enrolled. Eight participants were white (57%), and six were black (43%). Five participants (36%) were living with HIV and engaged with HIV care services. Interview themes included preference for sexual healthcare environments specializing in LGBTQ+ care, enthusiasm toward at-home STI testing, an emphasis on affirming patient-provider interactions in sexual healthcare settings, a preference for sexual healthcare providers involved in STI testing who were not cisgender men, and gender dysphoria around sexual health discussions and testing. Transgender women in the Southeastern US prioritize affirming provider-patient interactions, however resources in the region are limited. Participants were enthusiastic about at-home STI testing options, which have the potential to mitigate gender dysphoria. Further investigation into development of remote sexual healthcare services for transgender women should be performed.

Perspectives and Experiences on Engaging in Physical Activity for Adults with Intellectual Disabilities

Physical activity [PA] benefits all individuals, especially those with intellectual disabilities [ID]. This study explores the lived perspectives and experiences of PA for individuals with ID. Two focus groups (n = 8; n = 12) were conducted with participants enrolled in a postsecondary program at an institution of higher education [IHE] postsecondary education. The focus group was conducted on Zoom. Audio recordings were transcribed using NVivo 12, a qualitative software for themes and subthemes. Three main themes emerged: motivation, self-efficacy, and fitness considerations. Several subthemes within each theme emerged to support the main themes. Application of health education and opportunities to engage in physical activities [PAs], education of PA facility capacities to assist all adults, and community health-related supports may improve the retention of participating in PAs for all.

Research and scholarly methods: Thematic analysis

AbstractThematic analysis (TA) is a commonly used approach in qualitative research. TA has been widely applied in various disciplines such as psychology, sociology, and anthropology, and is now increasingly employed in pharmacy and healthcare research. However, pharmacy researchers may not be familiar with TA. The objectives of this manuscript are to succinctly describe the process for TA explained through the six steps of Braun and Clark as it applies to pharmacy or healthcare‐related research, discuss how rigor is achieved in qualitative studies, provide an overview of the qualitative software that is available to assist with TA, and offer comparisons to quantitative analysis where appropriate to demonstrate the contrast with qualitative techniques such as TA.

Provider and client perspectives on the use of maternity waiting homes in rural Rwanda

ABSTRACT Background The World Health Organization recommends the implementation of maternity waiting homes (MWH) to reduce delays in access to obstetric care, particularly for high-risk pregnancies and mothers living far from health facilities, and as a result, several countries have rolled out MWHs. However, Rwanda has not implemented this recommendation on a large scale. There is only one MWH in the country, hence a gap in knowledge regarding the potential utilisation and benefits of MWHs. Objective To explore providers’ and clients’ perspectives on facilitators and barriers to the use of MWH in rural Rwanda. Methods We conducted a qualitative study to explore health providers’ and clients’ perspectives on facilitators and barriers to the use of MWH in Rwanda, between December 2020 and January 2021. We used key informant interviews and focus group discussions to collect data. Data were analysed using NVivo qualitative analysis software version 11. Results Facilitators included perceptions that the MWH offered either a peaceful and home-like environment, good-quality services, or timely obstetric services, and was associated with good maternal and neonatal outcomes. Barriers included limited awareness of the MWH among pregnant women, fear of health providers to operate the MWH at full capacity, women’s lack of autonomy, uncertainty over funding for the MWH, and perceived high user fees. Conclusion The Ruli MWH offers a peaceful environment for pregnant women while providing quality and timely obstetric care, resulting in positive maternal and neonatal outcomes for women. However, its existence and benefits are not widely known, and its use is limited due to inadequate resources. There is a need for increased awareness of the MWH among healthcare providers and the community, and lessons from this MWH could inform the scale up of MWHs in Rwanda.

Southeastern US anesthesia providers’ perspectives on abortion provision: Inductive findings from a qualitative study

ObjectivesHealth care providers, including anesthesia providers, hold varied personal views on abortion, which influences their involvement in multidisciplinary abortion care. We aimed to explore Southeastern US anesthesia providers’ perspectives on abortion provision and factors impacting their decision to provide anesthesia for hospital-based induced abortion. Study designWe conducted in-depth, individual interviews with currently practicing anesthesia providers in the Southeastern United States. We recruited participants from regional anesthesiology conferences and via snowball sampling. A semistructured interview guide explored domains of obstetric experiences, standardized abortion cases, and personal abortion attitudes. We coded data iteratively and analyzed data thematically using inductive approaches with qualitative software. ResultsFifteen participants completed interviews, at which point thematic saturation occurred. Participants represented a range of provider type and prior abortion experience. Participants weighed “personal and professional viewpoints” in considering their willingness to provide anesthesia care for hospital-based abortion. Many participants who personally disagreed with some abortion indications were still willing to provide anesthesia in those cases, some implicitly naming principles of medical ethics to justify differing professional and personal opinions. Participants also considered their “role in abortion decision-making”: all participants reported that the abortion decision belongs to the patient or their obstetrician and not the anesthesia provider. ConclusionsSoutheastern US anesthesia providers are influenced by multiple factors when considering their participation in hospital-based abortion care. Acknowledging differences in professional and personal viewpoints and identifying roles in abortion decision-making might be important to engaging anesthesia providers in abortion care, especially for high-risk medical or fetal indications. ImplicationsThis original, qualitative study identified several inductive themes that characterize how Southeastern US anesthesia providers formulate their level of participation in hospital-based abortion care. Acknowledging differences in professional and personal viewpoints and identifying roles in abortion decision-making might facilitate interdisciplinary abortion care, especially for high-risk medical or fetal indications.

Online Appendix for Qualitative software engineering research – reflections and guidelines

Online Appendix for Qualitative software engineering research – reflections and guidelines

Naloxone analogy and opioid overdose terminology preferences among rural caregivers: Differences by race

BackgroundDespite national and state policies aimed at increasing naloxone access via pharmacies, opioid overdose death rates rose during the COVID-19 pandemic, particularly among Blacks and American Indians (AIs) in rural areas. Caregivers, or third parties who can administer naloxone during an overdose event, are important individuals in the naloxone administration cascade, yet no studies have explored rural caregivers’ opioid overdose terminology and naloxone analogy preferences or whether these preferences differ by race. ObjectivesTo identify rural caregivers’ overdose terminology and naloxone analogy preferences and determine whether preferences differ by race. MethodsA sample of 40 caregivers who lived with someone at high risk of overdose and used pharmacies in 4 largely rural states was recruited. Each caregiver completed a demographic survey and a 20- to 45-minute audio-recorded semi-structured interview that was transcribed, de-identified, and imported into a qualitative software package for thematic analysis by 2 independent coders using a codebook. Overdose terminology and naloxone analogy preferences were analyzed for differences by race. ResultsThe sample was 57.5% white, 35% Black, and 7.5% AIs. Many participants (43%) preferred that pharmacists use the term “bad reaction” to refer to overdose events over the terms “accidental overdose” (37%) and “overdose” (20%). The majority of white and Black participants preferred “bad reaction” while AI participants preferred “accidental overdose.” For naloxone analogies, “EpiPen” was most preferred (64%), regardless of race. “Fire extinguisher” (17%), “lifesaver” (9.5%), and other analogies (9.5%) were preferred by some white and Black participants but not AI participants. ConclusionOur findings suggest that pharmacists should use the “bad reaction” term and “EpiPen” analogy when counseling rural caregivers about overdose and naloxone, respectively. Caregivers’ preferences varied by race, suggesting that pharmacists may want to tailor the terminology and analogy they use when discussing naloxone with caregivers.

Enablers and barriers to effective HIV self-testing in the private sector among sexually active youths in Nigeria: A qualitative study using journey map methodology.

HIV is a public health burden in Nigeria. HIV self-testing is one of the approaches to testing, which is the first of the 95:95:95 cascade of a coherent response to the epidemic. The ability to self-test HIV is influenced by various factors that can either serve as enablers or barriers. Exploring these enablers and barriers to the uptake of HIVST will help achieve optimal HIV self-testing and provide a deeper understanding of the HIVST kits users' journey. The purpose of the study was to identify enablers and barriers to the uptake of HIV self-testing among sexually active youth in Nigeria using journey map methodology. We conducted a qualitative exploratory study between January 2021 to October 2021 to understand the journey map for taking up and using HIVST in the private health delivery systems which include the pharmacies and PPMVs. 80 youths in Lagos, Anambra and Kano states were interviewed using IDIs and in-person FGDs. Their responses were audio-recorded, transcribed and analyzed using a qualitative software package (Nvivo software). A journey map for taking up and effectively using HIVST using the private sector among sexually active youths using key enablers and barriers at the attract, purchase, use, confirmation, linkage, and reporting stage was developed. The major enablers among participants were privacy and confidentiality, bundling purchases with other health products, easy-to-use instructions, and past experience with other self-testing kits. The major barriers were fear of discrimination, big packaging, high price, lack of confidence from user error and fear of status disclosure. Sexually active young people's perspectives enhance our understanding of the barriers and enablers of using HIVST through the private sector. Optimizing the enablers such as improved confidentiality that may be seen in e-pharmacy, reducing barriers and factoring sexually young people's perspectives will enhance the market and the uptake of HIVST towards ensuring sustainability and accelerating progress towards the 95-95-95 targets.

Towards a taxonomy of research areas in open government data

PurposeThis study aimed to develop a taxonomy of research areas in open government data (OGD) through a bibliometric mapping tool and a qualitative analysis software.Design/methodology/approachIn this study, the authors extracted metadata of 442 documents from a bibliographic database. The authors used a bibliometric mapping tool for familiarization with the literature. After that, the authors used qualitative analysis software to develop taxonomy.FindingsThis paper developed taxonomy of OGD with three research areas: implementation and management, architecture, users and utilization. These research areas are further analyzed into seven topics and twenty-eight subtopics. The present study extends Charalabidis et al. (2016) taxonomy by adding two research topics, namely the adoption factors and barriers of OGD implementations and OGD ecosystems. Also, the authors include artificial intelligence in the taxonomy as an emerging research interest in the literature. The authors suggest four directions for future research: indigenous knowledge in open data, open data at local governments, development of OGD-specific theories and user studies in certain research themes.Practical implicationsEarly career researchers and doctoral students can use the taxonomy to familiarize themselves with the literature. Also, established researchers can use the proposed taxonomy to inform future research. Taxonomy-building procedures in this study are applicable to other fields.Originality/valueThis study developed a novel taxonomy of research areas in OGD. Taxonomy building is significant because there is insufficient taxonomy of research areas in this discipline. Also, conceptual knowledge through taxonomy creation is a basis for theorizing and theory-building for future studies.

Barriers and facilitators to resilience for rural cancer survivors during COVID-19.

The purpose of this study was to identify the barriers and facilitators of resilience for rural cancer survivors during COVID-19. A descriptive qualitative study design was used to achieve the study objected. We recruited six posttreatment cancer survivors, four caregivers of cancer survivors, and one survivor who also identified as a caregiver, all from rural Southwest Virginia. Participants completed 60-90 minute virtual interviews that were recorded, transcribed, and verified in Dedoose qualitative software. Data was analyzed using an inductive and deductive coding strategies, and thematic analysis was used to develop key themes. Four key themes emerged from the data: 1) Religious faith is a primary source of resilience, 2) Spiritual cancer care strengthens resilience, 3) Virtual platforms provide critical connections to faith communities, and 4) Fearful and fatalistic cancer beliefs reduce resilience. The findings provide critical descriptive evidence that faith facilitates resilience for rural cancer survivors, while rural cultural norms of fearful and fatalistic cancer beliefs reduce resilience. In the context of COVID-19, rural survivors prioritize utilizing virtual support groups to strengthen their resilience. Nurses should incorporate a spiritual assessment into survivorship care, and guide survivors to existing virtual support groups.

Traditional Health Care Practitioners' Perspectives on Applying Informed Consent During African Traditional Medical Practice in Akwa Ibom State, Nigeria: A Cross-Sectional Qualitative Study.

Introduction: This study explored the perspectives of traditional health care practitioners (THPs) practicing in the areas of herbalism, bone setting, and traditional birth attendance, from Akwa Ibom state, Nigeria, on the possibility and implications of applying informed consent (IC) during African traditional medicine (ATM) practice. Methods: Semistructured interviews were conducted with 11 THPs, consisting of 5 herbalists, 3 traditional bone setters (TBS), and 3 traditional birth attendants (TBAs), who represented the diverse groups that the study intended to cover. In-depth interviews were conducted using a semistructured guide and were recorded, transcribed, and analyzed using thematic analysis with the assistance of NVivo® qualitative analysis software. Results: Participants were seven males (64%) and four females (36%), 35-67 years of age, with 5-25 years of experience as THPs. Forty-six percent of participants were herbalists (27%), TBS, and TBAs (27%). Most participants (82%) were Annang, and (18%) were Ibibio first-language speakers. Three major themes emerged from the data analysis: (i) Existing ethical framework related to IC, (ii) knowledge of consent, and (iii) application of IC during traditional medical practice. These themes and relevant subthemes were explored. All (100%) THPs agreed that it was essential to communicate risks and benefits while allowing patients to ask questions before treatment. All participants (100%) stated that risk communication is essential in ATM, whereas 36% said they communicated all therapy benefits to their patients. Respondents believed patients could make an informed choice if they had complete information disclosure. However, THPs in this study had limited knowledge of formal IC rules and regulations. Conclusions: This study revealed that THPs in this setting disclose a diagnosis, risks, some benefits, and treatment options to patients. Consent/agreement was obtained verbally and voluntarily during ATM practice, consistent with IC doctrine. THPs had limited knowledge of the critical elements of IC. However, they suggested that a form of IC that does not conflict with traditional African norms could be applicable in ATM. IC could facilitate documentation and help reduce risks in ATM practice.

Digital Curation in Qualitative Analysis Software: Analysis of the Training Process of Researchers

Digital Curation in Qualitative Analysis Software: Analysis of the Training Process of Researchers

COVID-19 Anti-Vaccine Sentiments in Malaysia: Narratives of Comments from Facebook Post.

The anti-vaccination movement was an ongoing issue in Malaysia, a Muslim-majority country, even before the COVID-19 pandemic. It is unclear whether the introduction of new COVID-19 vaccines would similarly provoke anti-vaccine sentiments. This study analyzed COVID-19 anti-vaccine sentiments in the Malaysian community. Anti-vaccine comments from Facebook page posts were extracted. The qualitative software QSR-NVivo 10 was used to manage, code and analyze the data. The fast-track COVID-19 vaccine evoked the fear of unknown long-term effects, safety, effectiveness and the duration of protection. The halal status of the COVID-19 vaccines is important. Although it is permissible to use vaccines that are not certified halal under the state of darurah (emergency), there was doubt that the current state has reached the stage of darurah that warrants the use of vaccines. COVID-19 vaccine microchip conspiracy theories were raised. COVID-19 is viewed as only severe for vulnerable populations, and hence vaccination is not needed for the healthy. There were opinions that coronavirus treatments would be more beneficial than vaccination. The anti-COVID-19 vaccine sentiments uncovered in this study provide important insights for the formulation of public health messages to instill confidence in new COVID-19 vaccines. Despite the pandemic being nearly over and many people worldwide having received COVID-19 vaccines, the findings provide important insight into potential issues regarding the introduction of new vaccines in the event of future pandemics.

"But I Live Here Too": Social-structural stressors, racial discrimination, and resiliency among urban dwelling black emerging adult men.

For many Black emerging adult men in the United States, social-structural stressors rooted in racial discrimination are daily experiences that place them at greater risk for poor health. Emerging adulthood is a critical life course period marked by greater experimentation with health risk behaviors. Although Black men's health vulnerabilities during this period are connected to their social-structural environments, investigations of these factors among noncollege sampled Black men remain limited. We conduced thirty semi-structured in-depth interviews to examine associations between social-structural challenges and social-structural resources for resiliency. Interviews were audio-recorded, transcribed verbatim, and coded using Dedoose web-based qualitative software. Through open coding, emergent concepts were connected across interviews and major themes were identified. We found three core social-structural stressors: (1) Racial profiling, (2) neighborhood violence, and (3) lack of economic opportunities, and three resilience factors: (1) Positive social networks, (2) community-based resources, and (3) safe environments that foster a sense of community. Collectively, these findings provide insight into developing structural- and community-level interventions tailored to bolster resiliency across multiple levels and counteract the social-structural challenges that young Black men face.

Professional translators’ and interpreters’ views on information competence: An exploratory qualitative study from the Spanish context

Information competence is essential in professional translation and interpreting. This paper gathers the views of professional translators and interpreters in Spain on information competence, by means of an exploratory qualitative study. A questionnaire composed essentially of open-ended questions was applied to gather data and the qualitative analysis software ATLAS.ti was used to code the results using thematic content analysis methods. The views provided by a sample of professional translators and interpreters ( n = 156) on the importance of information competence were collected, together with their recommendations on this key competence for those who are starting their training in translation and interpreting. The study also explores the main information needs highlighted by professionals, the sources of information they use most frequently and how they verify information, and their opinions on the gender perspective (with explicit mention of inclusive language) as part of information competence in professional practice. The results show that professionals consider information competence to be absolutely essential in the framework of translation competence, and recommend reinforcing information literacy training in university undergraduate degree programmes. They have multiple information needs (from terminological to contextual) that make them turn to a wide range of information resources (mainly personal sources and online documentary resources), but they need to strengthen their knowledge for information evaluation. Regarding the gender perspective, professionals practically limit their answers to their opinions on inclusive language and, although most of them are in favour, some resistance is detected. From the diagnosis carried out in this research, opportunities for supporting information literacy instruction in undergraduate degrees and in continuing professional development are identified.

Self-employment, illness, and the social security system: a qualitative study of the experiences of solo self-employed workers in Ontario, Canada

BackgroundToday’s labor market has changed over time, shifting from mostly full-time, secured, and standard employment relationships to mostly entrepreneurial and precarious working arrangements. Thus, self-employment (SE) has been growing rapidly in recent decades due to globalization, automation, technological advances, and the recent rise of the ‘gig’ economy, among other factors. Accordingly, more than 60% of workers worldwide are non-standard and precarious. This precarity profoundly impacts workers’ health and well-being, undermining the comprehensiveness of social security systems. This study aims to examine the experiences of self-employed (SE’d) workers on how they are protected with available social security systems following illness, injury, and income reduction or loss.MethodsDrawing on in-depth interviews with 24 solo SE’d people in Ontario (January – July 2021), thematic analysis was conducted based on participants’ narratives of experiences with available security systems following illness or injury. The dataset was analyzed using NVIVO qualitative software to elicit narratives and themes.FindingsThree major themes emerged through the narrative analysis: (i) policy-practice (mis)matching, (ii) compromise for a decent life, and (iii) equity in work and benefits.ConclusionsMeagre government-provided formal supports may adversely impact the health and wellbeing of self-employed workers. This study points to ways that statutory social protection programs should be decoupled from benefits provided by employers. Instead, government can introduce a comprehensive program that may compensate or protect low-income individuals irrespective of employment status.

An Exploratory Study on Measuring Teachers’ and Students’ Motivation for Craftsman Spirit in Higher Vocational Colleges

Skilled people with craftsman spirit are a high-quality human resource for companies. It is described in detail in Chinese government documents and there is a growing body of local research, but very little research in the international academic arena. This study traces the origins of craftsman spirit and what it involves in research. A literature review of the connotations and dimensions of craftsman spirit is conducted to explore the empirical research methodology of craftsman spirit. In the manufacturing sector, semi-structured interviews were conducted with 11 professional leaders with the title of 'craftsman' and the data collected was analysed in Qualitative Analysis Software. The study concludes with the development of a measurement concept to motivate teachers and students to develop craftsman spirit, which is applicable to Chinese higher vocational colleges.