ChiCTR2300069838Not yet recruitingNot Applicable
助听器对听障老年人抑郁状况的干预研究
国家或省自然科学基金1 site in 1 countryStarted: May 1, 2023Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Locations
- 1
- Primary Endpoint
- 抑郁状况
Study Overview
Brief Summary
助听器对听障老年人抑郁情绪的干预效果评估
Study Design
- Study Type
- 干预性研究
- Primary Purpose
- 随机平行对照
- Masking
- 单盲
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1.年龄 60 岁及以上(WHO 的老龄标准,也是我国典型的退休年龄);
- •2.临床上显著双耳听力障碍患者。通过双耳纯音测听检查后,双耳中听力较好一侧的实际听力损失 >=30 dB and<70 dB。听力阈值取 0.5、1.0、2.0、4.0KHz 四个频率所测值的平均值;
- •3.GDS-15 量表得分>=5 分;
- •4.认知功能保持完整。MoCA 量表得分>=26 分,确保被试者有能力参与研究;
- •5.耳部检查(耳廓、外耳道、鼓膜)正常,听力和耳科检查结果显示可以佩戴耳背式助听器;
- •6.愿意签署知情同意书。
Exclusion Criteria
- •1.极重度听力障碍患者。根据文献调查,患有极重度听力障碍的患者往往无法从助听器中有效获得听力补偿,对于这类患者,目前比较有效的治疗途径是人工耳蜗植入;
- •2.患有先天性听力障碍、基础性耳部疾病、鼓膜穿孔、听骨链异常、分泌性或化脓性中耳炎、听神经肿瘤、梅尼埃综合征、耳道闭锁等不适合佩戴助听器的患者,以及具有既往耳毒性药物使用史、既往噪声接触史、既往耳科手术史的患者;
- •3.患有严重耳鸣、单侧突发性听力损失且病程<3 个月、单侧听力损失伴随眩晕的患者;
- •4.过去一年内曾经接受或正在接受某种听力干预治疗的患者;
- •5.不符合 WHO 助听器佩戴标准的听障患者;
- •6.在过去的 6 个月内患有狂躁症、精神病、酒精滥用或依赖的患者。这些评估依据国际神经精神访谈 MINI 结果;
- •7.有急性自杀风险的患者。如果发现听障老年人存在高自杀风险,研究人员将建议其立即转诊到精神专科进一步诊断或通知病人家属;
- •8.患有严重致残综合病症的患者。如患有晚期癌症、肝性脑病、终末期肺病等严重致残病症,或有脑外伤、脑手术及桥小脑占位病变等病史的患者;
- •9.伴有急性上呼吸道感染的患者。
Arms & Interventions
干预组
对照组
Outcomes
Primary Outcomes
抑郁状况
听力状况
Secondary Outcomes
- 社会隔离
- 孤独感
- 基本日常生活能力
Investigators
Study Sites (1)
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