Elhoufey Amira
Department of Community Health Nursing, Alddrab University College, Jazan University, Jazan 45142, Saudi Arabia.
Med Sci (Basel). 2025 Jul 22;13(3):94. doi: 10.3390/medsci13030094.
This study aimed to assess the effect of educational programs on symptom severity for women at high risk of carpal tunnel syndrome (CTS). : A quasi-experimental design was applied. A purposive sample of 250 women at high risk of CTS was selected from the Faculty of Nursing, Assiut University, Egypt. Data collection instruments included a structured interview questionnaire and the Boston Carpal Tunnel Syndrome Questionnaire (BCTQ). : Most participants were middle-aged (41-50 years), married, and had higher education. At baseline, 61.2% of participants reported mild symptoms, 24.8% moderate, and 11.6% were asymptomatic. Following the educational program, symptom severity was significantly improved ( = 0.007). The proportion of asymptomatic participants increased from 11.6% to 20.4%, while those with moderate symptoms decreased from 24.8% to 6.4%. Functional status also improved significantly, with the percentage of participants reporting no difficulty increasing from 17.6% to 30% ( = 0.008). We found a significant reduction in symptom severity scores ( = 0.05) and functional impairment ( = 0.008). The educational program effectively reduced CTS symptoms and improved hand function, demonstrating its potential as a preventive and therapeutic intervention for women at high risk of CTS. However, this study's quasi-experimental design without a control group and a short follow-up period limits conclusions regarding long-term effectiveness and causal inference.
本研究旨在评估教育项目对腕管综合征(CTS)高危女性症状严重程度的影响。采用了准实验设计。从埃及阿斯尤特大学护理学院选取了250名CTS高危女性作为目的抽样样本。数据收集工具包括结构化访谈问卷和波士顿腕管综合征问卷(BCTQ)。大多数参与者为中年(41 - 50岁)、已婚且受过高等教育。基线时,61.2%的参与者报告有轻度症状,24.8%为中度,11.6%无症状。在教育项目实施后,症状严重程度有显著改善(P = 0.007)。无症状参与者的比例从11.6%增至20.4%,而中度症状者从24.8%降至6.4%。功能状态也显著改善,报告无困难的参与者比例从17.6%增至30%(P = 0.008)。我们发现症状严重程度评分(P = 0.05)和功能损害(P = 0.008)有显著降低。该教育项目有效减轻了CTS症状并改善了手部功能,证明其作为CTS高危女性预防和治疗干预措施的潜力。然而,本研究的准实验设计缺乏对照组且随访期较短,限制了关于长期有效性和因果推断的结论。