DDHA 8006 Week 8 Practice Inquiry Ethics Analysis Example

Doctor of Healthcare Administration Foundational Concepts Walden University Free custom sample in 24 to 48h

This DDHA 8006 Week 8 ethics analysis example examines a composed practice inquiry into unclosed specialty referrals for consent, identifiability and dual-role conflict, and states what each pressure does to the work. Walden DDHA 8006 asks DHA students to treat ethics as design rather than paperwork, and the inquiry, a 300-referral record trace, patient calls and staff interviews, is led by the organization's own director of operations. Kass and colleagues' critique of the research and treatment distinction and Lynn and colleagues on quality improvement ethics frame oversight by risk rather than label. Consent shapes nurse-led voluntary calls, identifiability shapes coded data and combined reporting and the dual role moves interviews to an outside colleague with process-level use of findings. A table records each pressure's cost, and Mehrotra and colleagues ground the stages traced.

CourseDDHA 8006 Doctor of Healthcare Administration Foundational Concepts
WeekWeek 8
Paper typeEthics analysis
LengthAbout 1,040 words, 6 pages
FormatAPA 7 student paper
SchoolWalden University
ProgramDoctor of Healthcare Administration (DHA)
UpdatedOctober 2026

Free sample paper for DDHA 8006 Week 8

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Consent, Identifiability and Two Hats: An Ethics Analysis of a Referral Completion Inquiry Led by the Organization's Own Director

Student Name

Walden University

DDHA 8006: Doctor of Healthcare Administration Foundational Concepts

Instructor Name

Month Day, Year

What this page is doingThe title names the three ethical pressures the analysis examines, including the dual role, which is the least obvious and most important.
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Consent, Identifiability and Two Hats: An Ethics Analysis of a Referral Completion Inquiry Led by the Organization's Own Director

The Inquiry Under Review

The practice inquiry developed in this course would study unclosed specialty referrals at Tallgrass Medical Group, a composite nine-practice primary care group. As designed, it would pull 300 referrals at random from twelve months of orders, trace each through scheduling, attendance and report return, stages drawn from a review of where referrals break down (Mehrotra et al., 2011), using the record, call specialist offices to confirm visits and call a subset of patients to ask why they did not attend. It would also interview eight to ten clinicians and staff about how referrals are handled. The person leading the inquiry is the group's director of operations, who is also a doctoral student. This analysis examines three ethical pressures on that design, consent, identifiability and dual role, and states what each pressure does to the work.

What this page is doingThe opening describes the inquiry concretely, so each ethical pressure can be tied to a specific activity.
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Is It Research or Quality Improvement?

The first question is which rules apply. Activities intended to improve care within an organization have traditionally been treated as quality improvement and handled through local oversight, whereas work meant to produce knowledge that travels beyond the organization has usually gone to an institutional review board as research. That distinction has been criticized as unstable, because many activities do both, and some scholars argue that ethical oversight should depend on the risks and burdens an activity imposes rather than on its label (Kass et al., 2013). An influential analysis of the ethics of quality improvement made a similar point: quality improvement can carry real risks to patients and staff, and should receive ethical review proportionate to those risks (Lynn et al., 2007).

This inquiry will be submitted to the university's review board because it is part of a doctoral program and its findings will be written up. But the analysis below would apply even if it were run purely as internal improvement, because the ethical pressures arise from what the inquiry does, not from what it is called.

Pressure 1: Consent

Tracing referrals through the record does not require contact with patients, and reviewing records for operations is a routine use of health information. Calling patients is different. A call from the organization asking why a patient missed a specialist appointment may feel intrusive, may be heard as blame and may reach a patient who did not attend for reasons they prefer to keep private, such as cost or fear of a diagnosis.

What this pressure does to the work: patient calls will open with a short script explaining the purpose, making clear the patient may say no and that saying no changes nothing about their care, and offering to arrange the missed appointment if the patient wishes. Calls will be made by a nurse rather than the director, so that patients hear from someone in a care role. Patients who decline will be recorded only as having declined. Staff interviews will use written consent, which is easier to give freely, though as discussed below, freedom is limited by the dual role.

Pressure 2: Identifiability

The sample will contain patients' names, diagnoses implied by specialty and in some cases sensitive specialties such as behavioral health or infectious disease. Staff interviews will reveal how particular practices handle referrals, which could identify individual employees, especially in small practices.

What this pressure does to the work: the dataset will be coded, with the key held separately, and behavioral health and infectious disease referrals will be excluded from the patient call subset to reduce the risk of disclosure. In reporting, practice-level findings will be combined so that no practice with fewer than four clinicians is reported alone. Quotations from staff will be checked to remove details that could identify the speaker. The cost of these protections is some loss of detail, for example the inability to compare the smallest practices, which the report will state as a limit.

Pressure 3: Two Hats

The most important pressure is the dual role. The person leading the inquiry is the director of operations, to whom many of the interviewees report directly or indirectly. Staff asked by their director how they handle referrals may not feel free to decline, and may describe what they think the director wants to hear rather than what they do. Findings that reflect poorly on a practice could, in principle, affect how that practice is managed. Patients, too, may feel differently about a call that they learn is part of a study by the organization's management.

What this pressure does to the work: staff interviews will be conducted by a doctoral colleague from outside the organization, using the same guide, and recordings will be transcribed and de-identified before the director sees them. Interviewees will be told in writing that participation will not affect evaluations and that the director will not know who declined. The director will not use any finding about an individual employee for personnel decisions; findings will be used only at the process level. Where the director is also the decision maker on changes, the analysis will be reviewed by the quality committee before changes are made, so that the director's interpretation is checked by others.

Table 1

Pressures and What They Do to the Work

PressureRiskChange to the designCost of the change
ConsentPatients feel blamed or pressuredScripted voluntary calls by a nurse; offer to rebookFewer completed calls
IdentifiabilitySensitive referrals or small practices identifiableCoded data; exclusions; combined reportingLess detail for small practices and sensitive specialties
Dual roleStaff not free to decline or speak candidly; findings used against individualsOutside interviewer; de-identified transcripts; process-level use only; committee reviewSlower analysis; director loses direct contact with interview data

Each pressure changes the design, and each change has a cost the report will acknowledge.

Conclusion

The referral inquiry raises three ethical pressures. Consent shapes how patients are contacted, identifiability shapes how data are held and reported and the dual role, the director studying the director's own organization, shapes who conducts interviews and how findings may be used. Each pressure changes the work and costs something. Naming those costs is part of conducting the inquiry ethically, because it tells readers what the findings can and cannot show.

What this page is doingThe conclusion links each pressure to a design consequence and a cost, which is the analysis the assignment asks for rather than a general statement of principles.
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References

Kass, N. E., Faden, R. R., Goodman, S. N., Pronovost, P., Tunis, S., & Beauchamp, T. L. (2013). The research-treatment distinction: A problematic approach for determining which activities should have ethical oversight. Hastings Center Report, 43(s1), S4-S15. https://doi.org/10.1002/hast.133

Lynn, J., Baily, M. A., Bottrell, M., Jennings, B., Levine, R. J., Davidoff, F., Casarett, D., Corrigan, J., Fox, E., Wynia, M. K., Agich, G. J., O'Kane, M., Speroff, T., Schyve, P., Batalden, P., Tunis, S., Berlinger, N., Cronenwett, L., Fitzmaurice, J. M., . . . James, B. (2007). The ethics of using quality improvement methods in health care. Annals of Internal Medicine, 146(9), 666-673. https://doi.org/10.7326/0003-4819-146-9-200705010-00155

Mehrotra, A., Forrest, C. B., & Lin, C. Y. (2011). Dropping the baton: Specialty referrals in the United States. The Milbank Quarterly, 89(1), 39-68. https://doi.org/10.1111/j.1468-0009.2011.00619.x

Reading the DDHA 8006 Week 8 instructions

Ethics analyses in doctoral administration courses ask you to examine a planned inquiry for ethical pressures and show how they change it. Describe the inquiry concretely: what data, from whom, collected by whom. Address whether it counts as research or quality improvement and why the label matters less than the risks. Then take each pressure in turn, such as consent, identifiability and dual role, and describe the risk, the change it forces in the design and the cost of that change. Give particular attention to your own position if you are studying your own organization. Summarize pressures, changes and costs in a table. Close by explaining how naming those costs affects what the findings can claim, since honest limits are part of conducting the inquiry ethically.

Inside the DDHA 8006 Week 8 example

The analysis opens by describing the inquiry and the director's dual role. A section discusses the research and quality improvement distinction, citing Kass and colleagues and Lynn and colleagues, and explains why the inquiry goes to review anyway. Three pressure sections follow. Consent leads to scripted voluntary calls by a nurse with an offer to rebook. Identifiability leads to coded data, exclusion of sensitive specialties from calls and combined reporting for small practices. The dual role leads to an outside interviewer, de-identified transcripts, process-level use and committee review. Table 1 sets out risks, changes and costs, and the conclusion links each pressure to a design consequence.

DDHA 8006 Week 8 rubric: what earns full marks

Ethics analyses are graded on specificity. Describing the inquiry concretely earns the foundation, since ethics must attach to real activities. A thoughtful treatment of the research and quality improvement question, grounded in literature, shows awareness of oversight debates. The core credit goes to showing how each pressure changes the design, not merely naming principles. Attention to the dual role, often overlooked, distinguishes stronger papers. Acknowledging the costs of safeguards shows honesty about trade-offs. A summary table aids review. References must support the ethical framework and appear in APA style. Marks also follow whether the safeguards are proportionate, since piling on review steps for a record trace with minimal risk can be as weak an answer as ignoring risk altogether.

Common DDHA 8006 Week 8 mistakes, and how to avoid them

Ethics papers often list principles such as respect and beneficence without touching the actual plan. Start with what you will do: whose records, whose phone calls, whose interviews. For each, ask what could go wrong for that person. Then change the plan and say what the change costs. If you work in the organization you are studying, think hard about who will feel free to say no to you. If you are planning a practice inquiry, our writers can help you analyze its ethical pressures and redesign it so your review board and your staff can trust it. Write the consent script or data rule out in full in an appendix if your instructor allows it, because a reviewer trusts a safeguard they can read more than one you describe.

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DDHA 8006 Week 8 questions, answered

Where can I find a free DDHA 8006 Week 8 sample paper?

The practice inquiry ethics analysis is posted on this page free of charge.

What three pressures does the DDHA 8006 Week 8 analysis examine?

Consent, identifiability and the dual role of a director studying their own organization.

How does consent change the design?

Patient calls are scripted, voluntary, made by a nurse and include an offer to rebook the missed appointment.

How is the dual role managed?

An outside colleague conducts interviews, the director sees only de-identified transcripts and findings are used for processes, not people.

Does the label research or quality improvement settle the ethics?

No. Oversight should match the risks and burdens the activity imposes, whatever it is called.