Digital computerised cognitive training for preventing cognitive decline among hypertensive patients: a study protocol for a multicentre randomised controlled trial (DELIGHT trial)

被引:2
|
作者
Kong, Yu [1 ,2 ]
Guo, Qian Hui [3 ]
Zhou, Le [1 ]
He, Liu [1 ,2 ]
Zeng, Yong [1 ]
Du, Xin [1 ,2 ,4 ]
Dong, Jian Zeng [1 ]
Jiang, Chao [1 ]
Wang, Ji Guang [3 ]
Ma, Chang Sheng [1 ]
机构
[1] Capital Med Univ, Beijing AnZhen Hosp, Natl Clin Res Ctr Cardiovasc Dis, Dept Cardiol,Off Beijing Cardiovasc Dis Prevent, Beijing, Peoples R China
[2] Heart Hlth Res Ctr, Beijing, Peoples R China
[3] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Hypertens, Ctr Epidemiol Studies & Clin Trials,Sch Med,Dept C, Shanghai, Peoples R China
[4] Univ New South Wales, Sydney, NSW, Australia
来源
BMJ OPEN | 2024年 / 14卷 / 02期
关键词
Hypertension; Delirium & cognitive disorders; Nephrology; CARDIOLOGY; IMPAIRMENT; DEMENTIA; PERFORMANCE; PEOPLE;
D O I
10.1136/bmjopen-2023-079305
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Mild cognitive impairment (MCI) is an important intervenable stage for the prevention of dementia. Hypertension is associated with impaired cognition, and when combined with MCI, it may lead to a poor prognosis. Digital computerised cognitive training (CCT) has recently become a potential instrument for improving cognition, but evidence for its efficacy remains limited. This study aims to evaluate the efficacy of a digital adaptive CCT intervention in older patients with hypertension and MCI. Methods and analysis The multicentre, double-blinded, randomised, actively -controlled clinical trial will recruit 200 older (>= 60 years) patients with hypertension and MCI from 11 hospitals across China. Participants will be randomly assigned in a 1:1 ratio to the intervention group (multidomain adaptative CCT) and active control group (non-adaptive cognitive training) for 12-week cognitive training for 30 min/day and 5 days/week. Those who have completed their 12-week training in the intervention group will be rerandomised into the continuation and discontinuation training groups. All participants will be followed up to 24 weeks. Neuropsychological assessments and structural and functional 7.0 T MRI will be obtained at baseline and at 12-week and 24-week follow-up. The primary outcome is the possible improvement of global cognitive function at 12 weeks, as measured by the Basic Cognitive Aptitude Tests. Secondary and exploratory endpoints include the major cognitive domain function improvement, self-efficacy, mental health, quality of life and MRI measurements of the brain. Ethics and dissemination The trial has been approved by the institutional review board of Beijing Anzhen Hospital and thereafter by all other participating centres. Trial findings will be disseminated in peer-reviewed journals and conference presentations. Trial registration number NCT05704270.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] ACTIB TRIAL (ASSESSING COGNITIVE BEHAVIOURAL THERAPY IN IRRITABLE BOWEL): A MULTICENTRE RANDOMISED CONTROLLED TRIAL
    Everitt, Hazel
    Landau, Sabine
    Little, Paul
    Bishop, Felicity
    O'Reilly, Gillian
    Sibelli, Alice
    Holland, Rachel
    Hughes, Stephanie
    Wingassen, Sula
    McCrone, Paul
    Goldsmith, Kim
    Coleman, Nicholas
    Logan, Robert
    Chlader, Trudie
    Moss-Morris, Rona
    GUT, 2018, 67 : A208 - A209
  • [32] COMBINING PHARMACOTHERAPY OF BI 425809 WITH COMPUTERISED COGNITIVE TRAINING IN PATIENTS WITH SCHIZOPHRENIA: INITIAL EXPERIENCE OF A LARGE-SCALE MULTICENTRE RANDOMISED CLINICAL TRIAL
    Hake, Sanjay
    Huang, Songqiao
    McDonald, Sean
    Pollentier, Stephane
    Podhorna, Jana
    SCHIZOPHRENIA BULLETIN, 2020, 46 : S47 - S47
  • [33] The socrates trial: A multicentre, randomised, controlled trial of cognitive-behaviour therapy in early schizophrenia
    Lewis, SW
    Tarrier, N
    Haddock, G
    Bentall, R
    Kinderman, P
    Kingdon, D
    Siddle, R
    Leadley, K
    Grazebrook, K
    Everitt, J
    Benn, A
    Faragher, B
    SCHIZOPHRENIA RESEARCH, 2000, 41 (01) : 9 - 9
  • [34] Computerised cognitive training to improve cognition including delirium following coronary artery bypass grafting surgery: protocol for a blinded randomised controlled trial
    Greaves, Danielle
    Psaltis, Peter J.
    Lampit, Amit
    Davis, Daniel H. J.
    Smith, Ashleigh E.
    Bourke, Alice
    Worthington, Michael G.
    Valenzuela, Michael J.
    Keage, Hannah A. D.
    BMJ OPEN, 2020, 10 (02):
  • [35] A randomised controlled trial of computerised cognitive behaviour therapy for the treatment of depression in primary care: the Randomised Evaluation of the Effectiveness and Acceptability of Computerised Therapy (REEACT) trial
    Littlewood, Elizabeth
    Duarte, Ana
    Hewitt, Catherine
    Knowles, Sarah
    Palmer, Stephen
    Walker, Simon
    Andersen, Phil
    Araya, Ricardo
    Barkham, Michael
    Bower, Peter
    Brabyn, Sally
    Brierley, Gwen
    Cooper, Cindy
    Gask, Linda
    Kessler, David
    Lester, Helen
    Lovell, Karina
    Muhammad, Usman
    Parry, Glenys
    Richards, David A.
    Richardson, Rachel
    Tallon, Debbie
    Tharmanathan, Puvan
    White, David
    Gilbody, Simon
    HEALTH TECHNOLOGY ASSESSMENT, 2015, 19 (101) : 1 - +
  • [36] Efficacy of digital cognitive behavioural therapy for symptoms of generalised anxiety disorder: a study protocol for a randomised controlled trial
    Gu, J.
    Miller, C. B.
    Henry, A. L.
    Espie, C. A.
    Davis, M. L.
    Stott, R.
    Emsley, R.
    Smits, J. A. J.
    Craske, M.
    Saunders, K. E. A.
    Goodwin, G.
    Carl, J. R.
    TRIALS, 2020, 21 (01)
  • [37] Efficacy of digital cognitive behavioural therapy for symptoms of generalised anxiety disorder: a study protocol for a randomised controlled trial
    J. Gu
    C. B. Miller
    A. L. Henry
    C. A. Espie
    M. L. Davis
    R. Stott
    R. Emsley
    J. A. J. Smits
    M. Craske
    K. E. A. Saunders
    G. Goodwin
    J. R. Carl
    Trials, 21
  • [38] A randomised controlled pilot trial protocol for patient led cognitive gamified training during haemodialysis
    Aksoy, Murat
    Hunter, Samantha
    Asghar, Aziz U. R.
    Bhandari, Sunil
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [39] Assessing the feasibility of a randomised controlled trial examining the effect of hearing aids on cognitive decline in elderly individuals: a study protocol
    Fuchten, Denise
    Smit, Adriana L.
    Wajer, Irene M. C. Huenges
    Rhebergen, Koen S.
    Stegeman, Inge
    BMJ OPEN, 2023, 13 (12):
  • [40] Effect of Baduanjin exercise on cognitive function in patients with post-stroke cognitive impairment: study protocol for a randomised controlled trial
    Zheng, Guohua
    Zheng, Yuhui
    Xiong, Zhenyu
    Ye, Bingzhao
    Tao, Jing
    Chen, Lidian
    BMJ OPEN, 2018, 8 (06):