Study A (approx. 600 words total)Verkleij, S., Luijsterburg, P., Willemsen, S., Koes, B., Bohnen, A., & Bierma - Zeinstra, S XXXXXXXXXXEffectiveness of diclofenac versus paracetamol in knee...

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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?









References





Answered 3 days AfterApr 29, 2023

Answer To: Study A (approx. 600 words total)Verkleij, S., Luijsterburg, P., Willemsen, S., Koes, B., Bohnen,...

Deblina answered on May 02 2023
35 Votes
Research Paper Analysis         2
RESEARCH PAPER ANALYSIS
Table of Contents

Study A    3
Study Design    3
Methods Used    3
Data Collection & Analysis    4
Results    4
Summary    5
Study B    5
Problem of the Study    5
Methodology    6
Recruitment & S
ample    6
Data Collection    7
Data Analysis    7
Summary    7
References    9
Study A
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 primary care. British Journal of General Practice, 65(637), e530-e537.
Study Design
The study has focus to contemplate the effectiveness of the diclofenac compared to that of paracetamol over a period of 2,4 and 12 weeks in the patients suffering from osteoarthritis. However, the research question and the research objectives are not distinctively mentioned in the research paper (Verkleij et al., 2015). However, the hypothesis which was to compare the effectiveness of the diclofenac versus paracetamol in treating me osteoarthritis as a primary care is mentioned.
PICO was used to define the research objectives. The population was the patients with knee osteoarthritis and the intervention was diclofenac and paracetamol. The comparison was between the two treatments of diclofenac and paracetamol. The outcome measures were pain intensity and the quality of life with the proper use of rescue medication.
The patients were randomized which focuses on the fat that the participants were randomly allocated to either diclofenac or Paracetamol group ensuring that the groups were similar in terms of baseline characteristics and this minimized the risk of selection bias.
Methods Used
The study appears to be methodologically sound. The study did not mention whether or not blinding occurred. The groups of the study where similar at the start of the study and the randomisation process have effectively help to ensure that the two groups were comparable in terms of the baseline characteristics. The potential propounding factors that could have affected the outcome were not mentioned. It is not clear from the paper if each study group received same standard of care apart from the intervention that was compared. It is possible that they are can be certain differences in terms of care received by each group which could have affected the outcomes. Similarly, earlier medical history of the patients can have a significant impact on the outcomes of the interventions on the groups which was not considered in the study. The paper however provided a clear description of the study protocol and the intervention criteria and follow up intervals were similar. The follow up intervals were same for both the study groups with outcome measures assessed at the baseline at 6 to 12 weeks. The sample size was appropriate for the study design and the primary care setting was appropriate for the given nature of the condition that are being studied.
Data Collection & Analysis
The instruments that were used to assess...
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