Instructions (delete all purple text prior to submitting):This assignment requires you to critically appraise two studies.Download this template, leave the sub-headings, and delete the purple text...

1 answer below »









Instructions (delete all purple text prior to submitting):











This assignment requires you to critically appraise two studies.








Download this template, leave the sub-headings, and delete the purple text prior to submission.








Ensure your student name and ID is included.








The assignment should be supported by a minimum of 8 references; however, you are encouraged to use more if needed to support your discussion. References should be valid academic sources.








Your appraisal should have in-text references as per APA 7th


referencing style. You do not need to reference the two studies that you are appraising – this has been done for you.









The word limit is 1200 words +/- 10%. This includes in-text citations but not the reference list or sub-headings.








Note that the section marked ‘consider’ are suggestions only, there is likely to be more detail that you should add.










































































































































































Study A (approx. 600 words total)





Verkleij, S., Luijsterburg, P., Willemsen, S., Koes, B., Bohnen, A., & Bierma - Zeinstra, S. (2015). Effectiveness of diclofenac versus paracetamol in knee osteoarthritis: a randomised controlled trial in primary care.

British Journal of General Practice, 65(637), E530–E537.

https://doi.org/10.3399/bjgp15X686101










Study design valid for a Randomised Control Trial








Consider: Did the study address a clearly focussed research question or hypothesis, was PICO used to define the question, was the assignment of participants randomised, were all participants that entered the study accounted for at its conclusion?











Methodologically sound








Consider: did ‘blinding’ occur, were the study groups similar at start of the study, could any differences affect the outcome, apart from the intervention did each study group receive the same standard of care, was there a clear study protocol, were follow up intervals the same for each group, is the sample and setting appropriate?











Data collection, instruments, analysis







Consider: What instruments were used to collect data, were they appropriate for the study, how was the data analysed?











Results








Were the effects of the intervention reported comprehensively?














Summary









Consider: What is your conclusion about the paper? Would you use it to change your practice or to recommend changes to care? Strengths and limitations?

























































































Study B (approx. 600 words total)





Bak, M. A. R., Hoyle, L. P., Mahoney, C., & Kyle, R. G. (2020). Strategies to promote nurses’ health: A qualitative study with student nurses.

Nurse Education in Practice, 48, 102860.

https://doi.org/10.1016/j.nepr.2020.102860










Problem the study was designed to solve








Consider: Is there a clear statement of the aim, why was it thought important to conduct this study?











Qualitative methodology appropriateness








Consider: what type of study design was used, was it appropriate to answer the research question, did the authors justify the research design?











Recruitment and sample








Consider: how were participants selected, were the sample’s characteristics appropriate based on the design and setting of the study?











Data collection








Consider: Was the setting for collection justified, is it clear how it was collected, were tools or instrument used, were they appropriate based on study design, is the form of the data clear (e.g., recordings, video etc)?











Data analysis rigor








Consider: is an in-depth description of the analysis process given; is sufficient data presented to support findings; are contradictory data considered; has the researcher examined their own role, potential bias, and influence during analysis and collection of data?











Summary





Consider: What is your conclusion about the paper? Would you use it to change your practice or to recommend changes to care? Strengths and limitations?


Answered Same DayMay 06, 2023

Answer To: Instructions (delete all purple text prior to submitting):This assignment requires you to...

Dr Insiyah R. answered on May 07 2023
31 Votes
Study 1    1
Study 2    3
Study 1
Verkleij, S. P., Luijsterburg, P. A., Willemsen, S. P., Koes, B. W., Bohnen, A. M., & Bierma-Zeinstra, S. M. (2015). Effectiveness of diclofenac versus paracetamol in knee osteoarthritis: a randomised controlled trial in prima
ry care. British Journal of General Practice, 65(637), e530-e537.https://doi.org/10.3399/bjgp15X686101
The most common form of joint disease, osteoarthritis (OA), results in pain and functional impairment. According to estimates, symptomatic OA affects 18.0% of women and 9.6% of men over 60. Because of its higher safety profile, paracetamol is advised as the medicine of first choice when clinical practice guidelines for knee OA require pain treatment for OA. Non-steroidal anti-inflammatory medications (NSAIDs) may be used if paracetamol is ineffective in relieving pain. Significant cohort research, however, revealed that most patients chose NSAIDs over paracetamol. Furthermore, according to Ausiello and Stafford8, doctors recommended NSAIDs to more than 30% of patients, whereas paracetamol was only prescribed in 10% of visits for OA. The evidence for addressing OA was summarised, and NSAIDs had larger effect sizes than paracetamol. Due to its widespread availability, paracetamol may not be viewed as a medicine. The majority of earlier studies contrasted NSAIDs with paracetamol in carefully chosen participants who were already taking NSAIDs and required a washout period before randomisation. According to one study, past NSAID usage predicted a more significant response to NSAIDs compared to paracetamol. Additionally, most of the participants in earlier research were chosen from secondary care settings. Therefore, the purpose of this study was to examine the efficacy of diclofenac and paracetamol in treating individuals who have knee OA in general practice throughout periods of 2, 4, and 12 weeks. In general rule, a pragmatic open-labelled randomised controlled experiment was conducted. The study protocol's full details are published elsewhere. Patients who visited their general practitioners in the southwest of the Netherlands with a fresh bout of non-traumatic knee pain were recruited. In order to be considered a new episode of knee pain, a patient had to disclose their symptoms to their doctor for the first time in the preceding three months. Patients might participate provided they complied with all of the following requirements: age 45; new onset of non-traumatic knee pain; knee pain intensity of 2 or greater (on a 0–10 scale); and meeting the clinical requirements of...
SOLUTION.PDF

Answer To This Question Is Available To Download

Related Questions & Answers

More Questions »

Submit New Assignment

Copy and Paste Your Assignment Here