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Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial

Overview of attention for article published in Trials, December 2014
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Title
Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial
Published in
Trials, December 2014
DOI 10.1186/1745-6215-15-472
Pubmed ID
Authors

Johanna N Kues, Carolyn Janda, Maria Kleinstäuber, Cornelia Weise

Abstract

With a prevalence of 3 to 8% among women of reproductive age, severe premenstrual symptoms are very common. Symptoms range from emotional and cognitive to physical changes. Severe symptoms (that is, premenstrual syndrome) can have a strong impact on everyday functioning and quality of life. Impairment can be as serious as that of dysthymic disorders. Many affected women receive either no treatment at all or are unsatisfied with their treatment. Although there is some evidence for the reduction of distress through cognitive behavioural therapy, there are only a small number of randomised controlled trials carefully investigating the efficacy of this psychotherapeutic approach. Thus, this study aims to evaluate the efficacy of a cognitive behavioural self-help treatment for women suffering from premenstrual syndrome.Methods/design: The study is conducted as a randomised controlled trial. The complex diagnostic assessment includes the completion of a symptom diary over two consecutive cycles and a telephone interview. Eligible women are randomly assigned to either a treatment or a wait-list control group. The intervention is based on cognitive behavioural therapy principles and is provided via the internet. It consists of 14 different modules on which participants work over 8 consecutive weeks. In addition to written information, participants receive email feedback from a clinical psychologist on a weekly basis. Participants assigned to the wait-list receive the treatment after the end of the waiting period (8 weeks). The primary outcome measure is the Premenstrual Syndrome Impairment Measure. Secondary outcomes include the Premenstrual Syndrome Coping Measure, the Short-Form Social Support Questionnaire, the Questionnaire for the Assessment of Relationship Quality, and the Perceived Stress Scale. Data is collected during the premenstrual (luteal) phase at pre-treatment, post-treatment, and 6-month follow-up.

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Geographical breakdown

Country Count As %
Unknown 208 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 34 16%
Student > Ph. D. Student 26 13%
Researcher 22 11%
Student > Doctoral Student 19 9%
Student > Bachelor 19 9%
Other 33 16%
Unknown 55 26%
Readers by discipline Count As %
Psychology 61 29%
Nursing and Health Professions 25 12%
Medicine and Dentistry 24 12%
Social Sciences 13 6%
Computer Science 3 1%
Other 17 8%
Unknown 65 31%