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Internet-based cognitive behavioural therapy (iCBT) for perinatal anxiety and depression versus treatment as usual: study protocol for two randomised controlled trials
被引:16
作者:
Loughnan, Siobhan A.
[1
]
Newby, Jill M.
[2
]
Haskelberg, Hila
[1
]
Mahoney, Alison
[1
]
Kladnitski, Natalie
[1
]
Smith, Jessica
[1
]
Black, Emma
[3
]
Holt, Christopher
[4
,5
]
Milgrom, Jeannette
[4
,5
]
Austin, Marie-Paule
[3
]
Andrews, Gavin
[1
]
机构:
[1] UNSW, St Vincents Hosp, Sch Psychiat, CRUfAD, Level 4,OBrien Ctr,St Vincents Hosp, Sydney, NSW 2010, Australia
[2] UNSW Sydney, Fac Sci, Sch Psychol, 1302 Mathews Bldg, Kensington, NSW 2052, Australia
[3] St John God Hosp, Perinatal & Womens Mental Hlth Unit, 13 Grantham St, Burwood, NSW 2134, Australia
[4] Heidelberg Repatriat Hosp, PIRI, 300 Waterdale Rd, Heidelberg West, Vic 3081, Australia
[5] Heidelberg Repatriat Hosp, Melbourne Sch Psychol Sci, 300 Waterdale Rd, Heidelberg West, Vic 3081, Australia
来源:
关键词:
Perinatal;
Antenatal;
Postpartum;
Pregnancy;
Internet;
Online;
Cognitive behavioural therapy;
Treatment;
Depression;
Anxiety;
ANTENATAL RISK-FACTORS;
POSTNATAL DEPRESSION;
POSTPARTUM DEPRESSION;
WHOQOL-BREF;
PSYCHOMETRIC PROPERTIES;
PSYCHOLOGICAL DISTRESS;
SCREENING SCALES;
MIXED ANXIETY;
MENTAL-HEALTH;
VALIDATION;
D O I:
10.1186/s13063-017-2422-5
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: We aimed to evaluate the acceptability and efficacy of two brief, Internet-delivered cognitive behavioural therapy interventions-MUMentum Pregnancy (study 1) and MUMentum Postnatal (study 2)-in reducing maternal symptoms of anxiety, depression and overall psychological distress compared to usual care in the perinatal period. Methods/Design: Women who are pregnant (study 1) or < 12 months postpartum (study 2) with current clinically elevated symptoms of anxiety and/or depression according to validated self-report measures, will be recruited via the research arm of a not-for-profit clinical and research unit in Australia and randomised to the intervention group or treatment as usual control group. The minimum sample size for each study (alpha 0. 05; power 0.80 for a g of 0.80) was identified as 50 with at least 10% more to be recruited to account for expected attrition. The co-primary outcome measures are the Patient Health Questionnaire 9-item scale and Generalised Anxiety Disorder 7-item scale to measure depression and anxiety symptom severity, respectively, and will be administered at the following primary time-points: baseline; post treatment; and at one-month follow-up. Psychological distress will be measured according to the Kessler-10 psychological distress scale at each primary time-point and will also be completed before each lesson for those in the intervention group. The total trial period nine weeks for study 1 and 11 weeks for study 2. Program efficacy will be determined using intent-to-treat mixed models. Maintenance of gains will be assessed at one-month follow-up. Discussion: The current randomised controlled trial seeks to extend the literature by evaluating the efficacy of a self-help intervention for women in the perinatal period. If efficacious, the MUMentum programs have the potential to be easily disseminated via https://thiswayup. org. au/to large numbers of women across Australia as an intervention for women screening positive for anxiety, depressive or distress symptoms during pregnancy or postpartum.
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