The methodology chapter of a nursing dissertation is the one your examiners read most slowly, because it is where a study on nurses or patients earns its permission to exist. It is also the chapter with the most South African machinery in it: an ethics committee registered with the National Health Research Ethics Council, a provincial Department of Health approval routed through the National Health Research Database, a hospital chief executive, a nursing service manager and a unit manager, each of whom must say yes before you speak to a participant. Ten steps, in writing order, with the expected output of each.
Step 1: Get the faculty template and the ethics guideline your committee applies
Download your department’s chapter template before writing a word; they differ in where the paradigm, the setting and the ethics section sit. Then download the document your ethics committee measures you against: the National Department of Health’s South African Ethics in Health Research Guidelines: Principles, Processes and Structures, third edition, published in 2024 under section 72 of the National Health Act 61 of 2003. Aspects of the 2024 edition were under appeal at the time of writing, so check which version your committee cites in its own application form rather than assuming.
Output: the faculty template saved with your chapter headings already in place, and the guideline edition your committee names, cited in your reference list.
Step 2: Name the design in the vocabulary of the field
South African nursing research has its own design vocabulary, and using it tells the examiner you have read the local literature. The three designs behind most master’s dissertations:
| Design | Wording South African nursing dissertations use | Data | Analysis | Typical sample |
|---|---|---|---|---|
| Quantitative survey | Quantitative, descriptive, cross-sectional design | Validated questionnaire | Descriptive and inferential statistics | 80 to 300 nurses across units or facilities |
| Qualitative interview study | Qualitative, exploratory, descriptive and contextual design | Semi-structured individual interviews or focus groups | Tesch’s eight steps of open coding, with an independent co-coder | 8 to 20 participants, to data saturation |
| Mixed methods | Sequential explanatory or convergent mixed-methods design | Questionnaire followed by interviews, or both at once | Both, with an explicit integration step | Survey sample plus 8 to 15 interviews |
Two further designs appear often enough to name: the Delphi technique, for expert consensus on a competency framework or guideline, and action research, for practice-development studies in a single unit. Name the design you chose, cite the methodology text your department uses — Brink, Van der Walt and Van Rensburg’s Fundamentals of Research Methodology for Healthcare Professionals (Juta, fourth edition) and Botma, Greeff and Makhado’s Research in Health Sciences are the two South African standards — and name the design you rejected and why.
Output: one paragraph naming the paradigm, one naming the design in the field’s wording, one naming the rejected alternative.
Step 3: Describe the setting by level, not by name
The setting section describes the facility by its place in the health system: a primary healthcare clinic, a community health centre, a district, regional, tertiary or central hospital; in which province and district; public or private; with the bed count and nursing establishment if the facility permits. Most provincial approvals and hospital chief executives will ask you not to name the facility, so write the setting so that it can be anonymised without losing what an examiner needs to judge transferability.
If your study is in the private sector, say which hospital group and note that the group’s own research approval procedure applies in addition to your university committee. The setting section also describes the unit — a medical ward, a neonatal intensive care unit, a theatre complex, a clinic running an HIV programme — because the unit decides who your participants are and when they can be reached.
Output: a setting paragraph that a reader from another province could use to judge whether your findings would transfer to their facility.

Step 4: Define the population in the categories the Nursing Act uses
Your population is defined by registration category, and the categories are fixed by the Nursing Act 33 of 2005 and the South African Nursing Council: professional nurse, midwife, staff nurse, auxiliary nurse and auxiliary midwife. State which are included and why: a study of medication administration might exclude auxiliaries whose scope of practice does not cover it; a study of clinical supervision might be limited to professional nurses with two years in the unit. Write the inclusion and exclusion criteria as a list, each with a reason.
Then describe the sampling: for a survey, an all-inclusive sample of every eligible nurse when the population is small, otherwise stratified sampling by category or shift; for interviews, purposive sampling with the criterion stated. How many participants that means, and how to justify the number, is worked through in our answer to how many participants a dissertation needs.
Output: a population statement in Nursing Act categories, a criteria list with reasons, and a sampling paragraph with a target number and its justification.
Step 5: Describe the instrument, and say where it came from
For a quantitative study, the instrument is almost always a published, validated scale rather than one you wrote, and the methodology chapter must report its origin, its subscales, its published reliability and the permission you obtained to use it. The scales South African nursing students actually use, and the permission and translation questions each raises, are covered in our guide to which validated scale to use in a nursing research report.
For a qualitative study, the instrument is the interview guide: reproduce the central question and the probes, name the language of the interviews, and say who transcribed and, if needed, translated. If you interviewed in isiZulu or Sesotho and analysed in English, the translation step is part of your method and must be written up.
Output: an instrument subsection with origin, structure, reliability, permission and, for interviews, the guide and the language procedure.
Step 6: Pilot, and report what the pilot changed
Pilot the questionnaire on five to ten nurses from a unit that will not be in the main study, or run one or two pilot interviews. The point of reporting a pilot is what you changed afterwards: two items reworded because they were read as the same question, a probe added because participants kept raising a topic the guide did not reach, paper questionnaires chosen because the unit’s connectivity made an online form impractical.
Step 7: Write the data collection procedure as the gatekeeper chain, in order
This is the step that distinguishes a South African nursing methodology chapter from one written anywhere else. Data collection in a public facility runs through a fixed sequence of permissions, and your chapter should narrate that sequence as it happened, with dates.
- University ethics committee. Your faculty or health sciences research ethics committee, which must be registered with the National Health Research Ethics Council. Its clearance certificate, with its reference number, goes in the appendices. What the committee reviews and how long it takes is set out in our explainer on ethics clearance at a South African university.
- Provincial Department of Health. Applications for postgraduate research in public facilities are submitted on the National Health Research Database, the national repository used by the National Health Research Committee and the nine provincial health research committees. The Western Cape, for example, requires the ethics clearance certificate, the final protocol as a PDF and a completed research summary for managers, and states a processing time of six to eight weeks after the application reaches the relevant facilities and districts.
- The facility. Written permission from the chief executive officer of the hospital or the district manager for a clinic, and then from the nursing service manager.
- The unit. The unit manager, who decides when you may approach staff and where. Agree the times: handover is not one of them, and neither is the middle of a night shift.
- The participants. Individual informed consent, on the form your ethics committee approved, obtained by you and not by the unit manager, so that no nurse feels that participation was required by a superior.
Then describe the collection itself: where questionnaires were distributed and collected, how sealed boxes preserved anonymity, where interviews took place, how long they ran, how they were recorded. The whole sequence commonly takes four to six months; write it up as it happened, delays included.
Output: a numbered permission chain with reference numbers and dates, followed by the collection procedure written so that a stranger could repeat it.
Step 8: State the analysis method before you have the data
For a survey, name the software, the descriptive statistics for each variable, the inferential test for each objective and the significance level. The decision between tests is worked through in our guide to which statistical test to use for your dissertation.
For interviews, South African nursing dissertations overwhelmingly use Tesch’s eight steps of open coding, as described in Creswell, followed by a consensus discussion between the researcher and an independent co-coder. Name the co-coder’s qualification, describe the consensus meeting, and say whether you used software or coded by hand.
Output: an analysis subsection that maps each objective to its statistical test or its coding procedure.

Step 9: Write rigour in the vocabulary that matches your design
Quantitative studies report validity and reliability: the instrument’s content validity, its published and your own Cronbach’s alpha per subscale, and the steps taken against non-response and social desirability bias. Qualitative studies report trustworthiness, and in South African nursing that means Lincoln and Guba’s four criteria — credibility, transferability, dependability and confirmability — with authenticity added by many departments. For each criterion, state the strategy: prolonged engagement, member checking, dense description of the setting, an audit trail, reflexive notes, the independent co-coder. A two-column table of criterion and strategy is the accepted format.
Output: a rigour subsection, as a table where possible, with one strategy per criterion.
Step 10: Write ethics as decisions, and close with limitations
The ethics subsection is not a recital of principles; it records decisions. Which participants were vulnerable and what you did about it: patients require particular care, and nurses interviewed about their own managers need assurance that transcripts will never reach those managers. How consent was taken and by whom. How anonymity was preserved in a unit where everyone knows who was interviewed. Where recordings and transcripts are stored, for how long and under whose control, in terms of the Protection of Personal Information Act. What you would do if a participant disclosed unsafe practice.
Close the chapter with limitations that are methodological: a single facility, a self-report instrument, no night-shift staff in the sample. Limitations about the phenomenon belong in the discussion chapter.
Output: an ethics subsection written as decisions, and a limitations paragraph confined to method.
A worked Harvard reference for the methodology text
UCT, Wits, Pretoria, Stellenbosch and Unisa each publish their own Harvard variant, so check your guide; the shape below is the common core.
Reference list: Brink, H., Van der Walt, C. and Van Rensburg, G. (2018) Fundamentals of research methodology for healthcare professionals. 4th edn. Cape Town: Juta.
In text: A quantitative descriptive design was selected because the objectives required measurement of prevalence rather than exploration of meaning (Brink, Van der Walt and Van Rensburg, 2018).
The ethics guideline takes the same shape with a corporate author: National Department of Health (2024) South African ethics in health research guidelines: principles, processes and structures. 3rd edn. Pretoria: National Department of Health.
Getting the chapter drafted this month
A nursing methodology chapter is long because it is procedural: ten subsections, each with fixed content, several describing a process that took months. That is the kind of chapter Tesify drafts well. You supply the design, the setting, the instrument, the permission chain with its dates and the analysis method, and it produces the subsections in your faculty’s order, so that your evenings after a shift go to correcting a draft rather than facing a blank page. The bibliography tool holds every source you cite in your faculty’s Harvard variant, so the reference list matches the chapter at submission. There is a free plan.
Draft your nursing methodology chapter with Tesify
If the theory behind your question is not yet settled, that decision comes before this chapter, and our guide to choosing a theoretical framework for a master’s dissertation sets out the tests. And if your study sits in a school rather than a ward, the parallel permission chain for education research is in our guide to the methodology chapter of an education mini-dissertation.
Frequently asked questions
How long should the methodology chapter of a nursing master’s dissertation be?
Typically 5 000 to 8 000 words, or a fifth of the dissertation. Qualitative studies run longer because the trustworthiness and analysis subsections are more discursive. If your faculty guide sets a range, that overrides any general figure.
Do I need provincial Department of Health approval as well as university ethics clearance?
Yes, for any study in a public health facility. University ethics clearance is the first permission, not the only one. Postgraduate research applications are submitted on the National Health Research Database, and the provincial health research committee and then the facility must approve before you collect data.
How long does provincial health research approval take?
The Western Cape states six to eight weeks after the application reaches the relevant facilities and districts, provided the application is complete; incomplete applications are declined after a week of notification. Other provinces do not all publish a figure. Budget two to three months and start the application the day your ethics certificate arrives.
Can I research the unit where I work?
Usually, with conditions. Your ethics committee will want to see how you managed the power relationship, and colleagues should be recruited by someone other than you or through a process that lets them decline without your knowledge. Many students choose a neighbouring unit instead.
What is Tesch’s method and why do nursing dissertations use it?
Tesch’s eight steps are a procedure for open coding of transcripts, widely reproduced in Creswell’s research design texts and adopted across South African nursing departments because they are explicit and can be shared with an independent co-coder. The consensus discussion between researcher and co-coder is the part examiners look for.
Which ethics guideline should I cite?
The National Department of Health’s South African Ethics in Health Research Guidelines, third edition, 2024, unless your ethics committee’s application form names a different version. Parts of the 2024 edition were under appeal at the time of writing, so cite the edition your committee applies.
