Lambert Justin, Ghadry-Tavi Rouzbeh, Knuff Kate, Jutras Marc, Siever Jodi, Mick Paul, Roque Carolyn, Jones Gareth, Little Jonathan, Miller Harry, Van Bergen Colin, Kurtz Donna, Murphy Mary Ann, Jones Charlotte Ann
Faculty of Medicine, Southern Medical Program, University of British Columbia, Okanagan campus, Kelowna, BC, Canada.
Faculty of Medicine, Department of Surgery, Division of Otolaryngology, University of British Columbia, Okanagan campus, Kelowna, BC, Canada.
Trials. 2017 Jan 28;18(1):47. doi: 10.1186/s13063-017-1792-z.
Hearing loss (HL) is a disability associated with poorer health-related quality of life including an increased risk for loneliness, isolation, functional fitness declines, falls, hospitalization and premature mortality. The purpose of this pilot trial is to determine the feasibility and acceptability of a novel intervention to reduce loneliness, improve functional fitness, social connectedness, hearing and health-related quality of life in older adults with HL.
This 10-week, single-blind, pilot randomized control trial (RCT) will include a convenience sample of ambulatory adults aged 65 years or older with self-reported HL. Following baseline assessments, participants will be randomized to either intervention (exercise, health education, socialization and group auditory rehabilitation (GAR)) or control (GAR only) groups. The intervention group will attend a local YMCA twice a week and the control group once a week. Intervention sessions will include 45 min of strengthening, balance and resistance exercises, 30 min of group walking at a self-selected pace and 60 min of interactive health education or GAR. The control group will attend 60-min GAR sessions. GAR sessions will include education about hearing, hearing technologies, enhancing communication skills, and psychosocial support. Pre-post trial data collection and measures will include: functional fitness (gait speed, 30-s Sit to Stand Test), hearing and health-related quality of life, loneliness, depression, social participation and social support. At trial end, feasibility (recruitment, randomization, retention, acceptability) and GAR will be evaluated.
Despite evidence suggesting that HL is associated with declines in functional fitness, there are no studies aimed at addressing functional fitness declines associated with the disability of HL. This pilot trial will provide knowledge about the physical, mental and social impacts on health related to HL as a disability. This will inform the feasibility of a larger RCT and preliminary evidence about the initial effects of a novel, community-based, holistic intervention addressing both the negative psychosocial and functional physical effects of HL among older adults.
ClinicalTrials.gov, NCT02662192 . Registered on 14 January 2016.
听力损失(HL)是一种与健康相关生活质量较差有关的残疾,包括孤独、孤立、身体机能下降、跌倒、住院和过早死亡风险增加。这项试点试验的目的是确定一种新型干预措施在降低患有HL的老年人的孤独感、改善身体机能、社会联系、听力和健康相关生活质量方面的可行性和可接受性。
这项为期10周的单盲试点随机对照试验(RCT)将纳入一个便利样本,即年龄在65岁及以上且自我报告有HL的非卧床成年人。在基线评估之后,参与者将被随机分为干预组(运动、健康教育、社交活动和小组听觉康复(GAR))或对照组(仅GAR)。干预组将每周两次前往当地的基督教青年会,对照组每周一次。干预课程将包括45分钟的强化、平衡和阻力训练,30分钟的自主选择速度的集体步行,以及60分钟的互动健康教育或GAR。对照组将参加60分钟的GAR课程。GAR课程将包括听力、听力技术、增强沟通技巧和心理社会支持方面的教育。试验前后的数据收集和测量将包括:身体机能(步速、30秒坐立试验)、听力和健康相关生活质量、孤独感、抑郁、社会参与和社会支持。在试验结束时,将评估可行性(招募、随机分组、保留率、可接受性)和GAR。
尽管有证据表明HL与身体机能下降有关,但尚无旨在解决与HL残疾相关的身体机能下降问题的研究。这项试点试验将提供有关HL作为一种残疾对健康的身体、心理和社会影响的知识。这将为更大规模RCT的可行性提供信息,并提供关于一种新型的、基于社区的、全面干预措施对老年人HL的负面心理社会和身体机能影响的初步效果的证据。
ClinicalTrials.gov,NCT02662192。于2016年1月14日注册。