Study Results
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Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2018-05-30
2018-08-15
Brief Summary
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The objectives of this study are to know the effect of cranial therapeutic massage on insomnia, in order to improve the quality of life and the woman's corporal satisfaction, and to promote a better functioning and performance of the activities of daily life.
MATERIAL AND METHODS In this study, the investigators selected women aged between 45 and 60 years, who presented changes and symptoms characteristic of the menopausal period, accompanied by alterations in sleep. In addition, the inclusion criteria require that women have not had a menstrual period for one year.
Exclusion criteria are excessive stress, the use of medications to promote sleep and some type of contraindication to receive treatment.
Protocol design It consists of a randomized clinical trial, with a total of 50 participants (n = 50), divided into a control group (n = 25) and an experimental group (n = 25).
Intervention The experimental group is subjected to 1 session per week of manual cranial therapy consisting of massage and cranial relaxing techniques, with a duration of 30 minutes each session approximately, for 3 weeks and one month follow-up. Manual therapy consists of a prone and supine cranial massage.
The control group does not receive treatment, but they will be evaluated the same as the experimental group.
Evaluations Clinical interview Includes anthropometric data (age, weight and height). The quality of life questionnaire Sf-36 and the Menopause Rating Scale (MRS) that assesses the state of well-being of the menopausal woman through 11 simple answer questions.
The Pittsburg Quality of Sleep Questionnaire (PSQI) takes sleep habits into account during the last month. The PSQI contains a total of 19 questions, grouped into 10 questions. In all cases, a score of 0 would indicate ease of sleeping, while a score of 3 would be a severe difficulty.
On the other hand, the Sleep Journal also evaluates sleep habits, characteristics and sleep quality, but unlike the previous one, this questionnaire has to be answered daily by the patients.
The Perceived Stress Scale (PSS) is composed of 14 questions that relate to the level of stress perceived during the last month; The higher the score of each question, the higher the level of stress the person has.
The Body Satisfaction Questionnaire. 10 questions is which must be answered according to the state of health that best describes the person at that time.
The Patient Global Impression of Change Scale questionnaire assesses the sensation of change, in terms of quality of life and sleep, functionality and limitation to perform the activities of daily life, which the participant has experienced since the beginning of the treatment of this study.
Analysis of data The data obtained will be stored in a database (SPSS), with which the analysis of the data will also be performed.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
TREATMENT
DOUBLE
Study Groups
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Cranial massage
Manual cranial therapy consisting of massage and cranial relaxing techniques, lasting 30 minutes each session approximately, for 3 weeks and one month follow-up. Manual therapy consists of a prone and supine cranial massage.
Cranial massage
Manual cranial therapy consisting of massage and cranial relaxing techniques, lasting 30 minutes each session approximately, for 3 weeks and one month follow-up. Manual therapy consists of a prone and supine cranial massage.
Control Group
The control group does not receive treatment.
Control group
The control group does not receive treatment
Interventions
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Cranial massage
Manual cranial therapy consisting of massage and cranial relaxing techniques, lasting 30 minutes each session approximately, for 3 weeks and one month follow-up. Manual therapy consists of a prone and supine cranial massage.
Control group
The control group does not receive treatment
Eligibility Criteria
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Inclusion Criteria
* who have not experienced any menstrual cycle for at least one year.
* showing clear menopausal symptoms.
Exclusion Criteria
* that present contraindications to receive the treatment.
45 Years
60 Years
FEMALE
Yes
Sponsors
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University of Valencia
OTHER
Responsible Party
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GEMMA V ESPÍ LÓPEZ, PhD
Principal Investigator
Locations
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Faculty of Physiotherapy
Valencia, , Spain
Countries
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Other Identifiers
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ID0020
Identifier Type: -
Identifier Source: org_study_id
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