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Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial
BACKGROUND: 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 li...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265499/ https://www.ncbi.nlm.nih.gov/pubmed/25467540 http://dx.doi.org/10.1186/1745-6215-15-472 |
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author | Kues, Johanna N Janda, Carolyn Kleinstäuber, Maria Weise, Cornelia |
author_facet | Kues, Johanna N Janda, Carolyn Kleinstäuber, Maria Weise, Cornelia |
author_sort | Kues, Johanna N |
collection | PubMed |
description | BACKGROUND: 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. DISCUSSION: So far, there is no study investigating internet-based cognitive behavioural therapy for premenstrual syndrome. The programme approaches the problem of high prevalence in combination with severe impairment and insufficient treatment options. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01961479, 9 October 2013. |
format | Online Article Text |
id | pubmed-4265499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42654992014-12-15 Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial Kues, Johanna N Janda, Carolyn Kleinstäuber, Maria Weise, Cornelia Trials Study Protocol BACKGROUND: 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. DISCUSSION: So far, there is no study investigating internet-based cognitive behavioural therapy for premenstrual syndrome. The programme approaches the problem of high prevalence in combination with severe impairment and insufficient treatment options. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01961479, 9 October 2013. BioMed Central 2014-12-02 /pmc/articles/PMC4265499/ /pubmed/25467540 http://dx.doi.org/10.1186/1745-6215-15-472 Text en © Kues et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Kues, Johanna N Janda, Carolyn Kleinstäuber, Maria Weise, Cornelia Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
title | Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
title_full | Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
title_fullStr | Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
title_full_unstemmed | Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
title_short | Internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
title_sort | internet-based cognitive behavioural self-help for premenstrual syndrome: study protocol for a randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265499/ https://www.ncbi.nlm.nih.gov/pubmed/25467540 http://dx.doi.org/10.1186/1745-6215-15-472 |
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