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Objectives: To explore the theoretical justification for blinding in randomized trials and make recommendations concerning the implementation and interpretation of blinded randomized trials.
Study Design And Setting: A theoretical analysis was conducted of the potential for bias in randomized trials with successful blinding (ie, trials in which beliefs about allocation to treatment or control groups are independent of actual allocation). The analysis identified conditions that must be satisfied to ensure that blinding eliminates the potential for bias associated with beliefs about allocation.
Results: Even when beliefs about allocation are independent of actual allocation, they can still cause bias. The potential for bias is eliminated when the belief is uniformly one of complete ambivalence about allocation.
Conclusion: Even when blinding succeeds in making beliefs about allocation independent of actual allocation, beliefs about allocation may still cause bias. It is difficult to determine the extent of bias in any particular trial. Bias could be eliminated by establishing a state of complete ambivalence about the allocation of every trial participant, but universal ambivalence may be difficult to achieve and may reduce the generalizability of the trial's findings.
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http://dx.doi.org/10.1016/j.jclinepi.2014.02.001 | DOI Listing |
Pain
September 2025
Centre for Pain Research, University of Bath, Bath, United Kingdom.
One-fifth of adults who receive a total knee replacement (TKR) go on to develop chronic pain. The behavioural approach taken to find a solution to pain may vary from assimilative (pursuit of analgesia) to accommodative (acceptance of pain insolubility and adoption of alternative goals). A total of 313 patients participated in a trial of an enhanced care pathway for TKR reported pain at 3 months after surgery.
View Article and Find Full Text PDFOral Dis
September 2025
Stomatology Hospital, School of Stomatology, Zhejiang, University School of Medicine, Zhejiang Provincial Clinical Research Center for Oral Diseases, Key Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Hangzhou, Zhejiang, China.
Objective: To evaluate the effects of a Health Belief Model-based oral health management program on self-efficacy, oral health behaviors, and three periodontal clinical indicators among pregnant women.
Study Design: A randomized controlled trial was conducted with 65 participants randomly allocated to the intervention (n = 39) and control (n = 26) groups. The intervention included one face-to-face education, three video calls, two online lectures, and regular follow-up supervision in 1 month, while the control group received one face-to-face education.
Dementia (London)
September 2025
University of Haifa, Haifa, Israel.
IntroductionDementia is an escalating global concern driven by aging populations, significantly impacting Low-Middle-income countries like Albania. Formal caregivers face a unique set of ethical dilemmas and concerns when caring for individuals with dementia and their families. The lack of ethical guidelines and policies further complicates decision-making in these contexts.
View Article and Find Full Text PDFOral Surg Oral Med Oral Pathol Oral Radiol
July 2025
Department of Oral and Maxillofacial Surgery, S. V. S. Institute of Dental Sciences, Mahabubnagar, Telangana, India.
Objectives: Surgical extraction of the impacted mandibular third molar has undesirable side effects such as pain, swelling, bleeding, alveolar osteitis, and trismus. This study evaluates the efficiency of transcutaneous electronic nerve stimulation (TENS) in the control of perioperative pain and postoperative oedema & trismus after the surgical extraction of impacted mandibular 3rd molars.
Study Design: A prospective, comparative, randomized, double-blind controlled clinical study was conducted on 23 patients requiring surgical extraction of bilateral impacted mandibular third molars.
JMIR AI
August 2025
Department of General Internal Medicine and Psychosomatics, Heidelberg University, Im Neuenheimer Feld 410, Heidelberg, 69120, Germany, 49 62215632879.
Background: Online depression screening tools may increase uptake of evidence-based care and consequently lead to symptom reduction. However, results of the DISCOVER trial suggested no effect of automated results feedback compared with no feedback after online depression screening on depressive symptom reduction six months after screening. Interpersonal variation in symptom representation, health care needs, and treatment preferences may nonetheless have led to differential response to feedback mode on an individual level.
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