The e-mental health treatment in Stockholm myocardial infarction with non-obstructive coronaries or Takotsubo syndrome study (E-SMINC): a study protocol for a randomised controlled trial

被引:4
作者
Olsson, Erik M. G. [1 ]
Norlund, Fredrika [1 ]
Rondung, Elisabet [2 ]
Humphries, Sophia M. [1 ]
Held, Claes [3 ]
Lynga, Patrik [4 ,5 ]
Spaak, Jonas [6 ]
Sundin, Orjan [2 ]
Sundelin, Runa [4 ,5 ]
Leissner, Philip [1 ]
Kovamees, Lena [7 ]
Tornvall, Per [4 ,5 ]
机构
[1] Uppsala Univ, Dept Womens & Childrens Hlth, Uppsala, Sweden
[2] Mid Sweden Univ, Dept Psychol & Social Work, Ostersund, Sweden
[3] Uppsala Univ, Uppsala Clin Res Ctr, Dept Med Sci, Cardiol, Uppsala, Sweden
[4] Karolinska Inst, Dept Clin Sci & Educ, Stockholm, Sweden
[5] Soder Sjukhuset, Dept Cardiol, Stockholm, Sweden
[6] Karolinska Inst, Danderyd Univ Hosp, Dept Clin Sci, Stockholm, Sweden
[7] Swedish Heart & Lung Assoc, Stockholm, Sweden
关键词
MI NOCA; Takotsubo syndrome; Stress; Anxiety; Cognitive behavioural therapy; Internet-based intervention; Randomised controlled trial; HOSPITAL ANXIETY; DEPRESSION; STRESS; VERSION; SCALE;
D O I
10.1186/s13063-022-06530-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: In the aftermath of a myocardial infarction with non-obstructive coronary arteries (MINOCA) or Takotsubo syndrome (TS), patients commonly express high levels of stress and anxiety. Current treatment alternatives rarely address these issues. Methods: The study is a randomised controlled trial, where 90 patients with a discharge diagnosis of MINOCA or TS who also report symptoms of stress or anxiety will be randomised 2-6 weeks after their cardiac event. The treatment consists of 10 weeks of Internet-based cognitive behaviour therapy (CBT) and starts immediately after randomisation for the treatment group. The control group receives usual care. Main outcomes are symptoms of anxiety measured with the Hospital Anxiety and Depression scale, anxiety subscale, and perceived stress measured with the Perceived Stress Scale, 14-item version, 10 weeks after randomisation. Secondary measures include cardiac specific anxiety, symptoms of post-traumatic stress, quality of life, cortisol measured in hair and physiological stress responses (heart rate variability, blood pressure and saliva cortisol) during a stress procedure. Ten weeks after randomisation, the control group will also receive treatment. Long-term followup in the self-report measures mentioned above will be conducted 20 and 50 weeks after randomisation where the total group's development over time is followed, and the groups receiving intervention early versus late compared. Discussion: At present, there are no randomised studies evaluating psychological treatment for patients with MINOCA or TS. There is an urgent need for treatment alternatives aiming at relieving stress and anxiety considering the high mental stress and anxiety levels observed in MINOCA and TS, leading to decreased quality of life. CBT aiming at reducing mental stress has been shown to be effective regarding prognosis in patients with coronary artery disease. The current protocol describes a randomised open-label controlled trial evaluating an Internet-based CBT program for reduction of stress and anxiety in patients with increased mental stress and/or anxiety with a discharge diagnosis of either MINOCA or TS.
引用
收藏
页数:12
相关论文
共 24 条
  • [21] M.I.C.E—Mental Health Intervention for Children with Epilepsy: a randomised controlled, multi-centre clinical trial evaluating the clinical and cost-effectiveness of MATCH-ADTC in addition to usual care compared to usual care alone for children and young people with common mental health disorders and epilepsy—study protocol
    Sophie D. Bennett
    J. Helen Cross
    Anna E. Coughtrey
    Isobel Heyman
    Tamsin Ford
    Bruce Chorpita
    Rona Moss-Morris
    Sarah Byford
    Emma Dalrymple
    Colin Reilly
    Terence Stephenson
    Caroline Doré
    Sophia Varadkar
    James Blackstone
    Kashfia Chowdhury
    Poushali Ganguli
    Liz Deane
    Roz Shafran
    [J]. Trials, 22
  • [22] European COMPARative Effectiveness research on blended Depression treatment versus treatment-as-usual (E-COMPARED): study protocol for a randomized controlled, non-inferiority trial in eight European countries
    Annet Kleiboer
    Jan Smit
    Judith Bosmans
    Jeroen Ruwaard
    Gerhard Andersson
    Naira Topooco
    Thomas Berger
    Tobias Krieger
    Cristina Botella
    Rosa Baños
    Karine Chevreul
    Ricardo Araya
    Arlinda Cerga-Pashoja
    Roman Cieślak
    Anna Rogala
    Christiaan Vis
    Stasja Draisma
    Anneke van Schaik
    Lise Kemmeren
    David Ebert
    Matthias Berking
    Burkhardt Funk
    Pim Cuijpers
    Heleen Riper
    [J]. Trials, 17
  • [23] European COMPARative Effectiveness research on blended Depression treatment versus treatment-as-usual (E-COMPARED): study protocol for a randomized controlled, non-inferiority trial in eight European countries
    Kleiboer, Annet
    Smit, Jan
    Bosmans, Judith
    Ruwaard, Jeroen
    Andersson, Gerhard
    Topooco, Naira
    Berger, Thomas
    Krieger, Tobias
    Botella, Cristina
    Banos, Rosa
    Chevreul, Karine
    Araya, Ricardo
    Cerga-Pashoja, Arlinda
    Cieslak, Roman
    Rogala, Anna
    Vis, Christiaan
    Draisma, Stasja
    van Schaik, Anneke
    Kemmeren, Lise
    Ebert, David
    Berking, Matthias
    Funk, Burkhardt
    Cuijpers, Pim
    Riper, Heleen
    [J]. TRIALS, 2016, 17
  • [24] A randomised controlled trial to compare clinical and cost-effectiveness of an online parent-led treatment for child anxiety problems with usual care in the context of COVID-19 delivered in Child and Adolescent Mental Health Services in the UK (Co-CAT): a study protocol for a randomised controlled trial
    Lucy Taylor
    Sophie Giles
    Sophie Howitt
    Zoe Ryan
    Emma Brooks
    Lucy Radley
    Abigail Thomson
    Emily Whitaker
    Fauzia Knight
    Claire Hill
    Mara Violato
    Polly Waite
    Vanessa Raymont
    Ly-Mee Yu
    Victoria Harris
    Nicola Williams
    Cathy Creswell
    [J]. Trials, 23