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Applied Relaxation for Vasomotor Symptoms

Primary Purpose

Menopause, Hot Flashes

Status
Terminated
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Applied Relaxation (AR)
Sponsored by
Elizabeth Nedstrand
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Menopause focused on measuring Hot flashes, Vasomotor symptoms, Menopause, Applied Relaxation, Health Related Quality of Life, Salivary cortisol

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • postmenopausal women (at least 12 months since last menstrual bleeding occurred or in previously hysterectomised women a serum follicle-stimulating hormone (S-FSH) defined as postmenopausal level according to references at the local laboratory)
  • More or equal to 7 moderate to severe hot flashes or more or equal at 50 hot flashes per week according to a two-week screening diary
  • ability to understand and speak Swedish
  • freely given informed consent

Exclusion Criteria:

  • unstable thyroid or other metabolic disease
  • treatment with hormone therapy (HT) or other complementary- or alternative treatments treatment for menopausal-related symptoms
  • treatment with psychopharmacological drugs and/or sedatives d-un-treated psychiatric disease
  • frequently exercising women (≥ 2h high-intensity activities/week)

Sites / Locations

  • University Hospital, Dept of Obstetrics and Gynecology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Applied Relaxation (AR)

Untreated Control Group (CG)

Arm Description

The women assigned to CG will be told to act as an untreated control group i.e. not to use hormonal treatment, other alternative medication, natural remedies for hot flashes and even not acupuncture, mind-body therapies or intensive physical activity.

Outcomes

Primary Outcome Measures

Hot flashes average number and severity
The average number and severity of hot flashes/24 hours in self-registered diaries during the 12th week

Secondary Outcome Measures

Hot flashes
The average number and severity of hot flashes per 24 hours after 3 months follow-up.
Hot flashes reduction of hot flashes
The reduction of hot flashes in women defined as responders. Responders are defined as women with ≥50% reduction of hot flashes.
Health Related Quality of Life
The total score in the Women Health Questionnaire measured at 12th week and after 3 months follow-up.
Adverse Events
Adverse events documented by means of using open-ended questions at each contact.
Salivary cortisol
Three samples of salivary cortisol (at awakening, 30 minutes after awakening, and at bedtime)were collected at baseline, after 12 weeks and 3 months after "end-of-treatment"

Full Information

First Posted
December 6, 2011
Last Updated
May 10, 2012
Sponsor
Elizabeth Nedstrand
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1. Study Identification

Unique Protocol Identification Number
NCT01488864
Brief Title
Applied Relaxation for Vasomotor Symptoms
Official Title
Applied Relaxation for Vasomotor Symptoms in Postmenopausal Women - a Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Terminated
Why Stopped
Low drop-out rate and slow recruitment rate
Study Start Date
March 2007 (undefined)
Primary Completion Date
September 2010 (Actual)
Study Completion Date
September 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Elizabeth Nedstrand

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objectives of this study are to compare frequency and severity of moderate to severe vasomotor symptoms in postmenopausal women treated with applied relaxation (AR) with an untreated control-group (CG) and to investigate if Health Related Quality of Life improve in the AR-group compared to an untreated CG.To study if salivary cortisol excretion would change within the AR treated group compared with the control group.
Detailed Description
Approximately 70% of women in Europe and North America experience hot flashes and night sweats during the climacteric period. Many women abstain from hormonal therapy because of side effects or contraindications such as breast cancer or thrombosis. Different alternative therapies for alleviation of hot flashes are described in the literature. Both pharmacological treatments, different types of natural remedies, acupuncture, life-style changes and mind-body therapies are suggested as promising therapies. Applied relaxation (AR) is a technique influenced on cognitive behavioral therapy (CBT) using coping mechanism and conditioning. Previous study with healthy postmenopausal women showed promising results on hot flash frequency with an average decrease of more than 70 % with persisting effect three months after therapy and also HRQoL significantly increased probably due to better sleep and diminished vasomotor symptoms. But the method must be further investigated before strong evidence-based conclusion can be drawn. Cortisol is a potent stress hormone regulated by the hypothalamic-pituitary axis. The factors underlying how alternative treatment works and the mechanism underlying improvements in symptoms are not fully understood.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Menopause, Hot Flashes
Keywords
Hot flashes, Vasomotor symptoms, Menopause, Applied Relaxation, Health Related Quality of Life, Salivary cortisol

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Applied Relaxation (AR)
Arm Type
Experimental
Arm Title
Untreated Control Group (CG)
Arm Type
No Intervention
Arm Description
The women assigned to CG will be told to act as an untreated control group i.e. not to use hormonal treatment, other alternative medication, natural remedies for hot flashes and even not acupuncture, mind-body therapies or intensive physical activity.
Intervention Type
Behavioral
Intervention Name(s)
Applied Relaxation (AR)
Intervention Description
AR is a technique influenced on cognitive behavioral therapy using coping mechanism and conditioning. AR focuses on muscle relaxation, where breathing is used for the conditioning of the relaxation. AR implies participation in 10 group sessions during a period of 12 weeks. A therapist will see the women assigned to AR in a group consisted of 6-8 women. The weekly sessions will last for 60 minutes each and are based on a scheme from Öst. The women will be told to practice each component daily. During the first session a lecture about menopause and about theories of the mechanisms behind hot flashes will be given. The aim of applying AR in view of coping with vasomotor symptoms will be discussed. The group is given a rationale of applying AR as a coping technique for handling sudden unanticipated symptoms by quick calming down, and thus gaining control over the situation.
Primary Outcome Measure Information:
Title
Hot flashes average number and severity
Description
The average number and severity of hot flashes/24 hours in self-registered diaries during the 12th week
Time Frame
Baseline to 12 week after "start of treatment"
Secondary Outcome Measure Information:
Title
Hot flashes
Description
The average number and severity of hot flashes per 24 hours after 3 months follow-up.
Time Frame
Baseline to 3 months after "end of treatment"
Title
Hot flashes reduction of hot flashes
Description
The reduction of hot flashes in women defined as responders. Responders are defined as women with ≥50% reduction of hot flashes.
Time Frame
Baseline to 3 months after "end of treatment"
Title
Health Related Quality of Life
Description
The total score in the Women Health Questionnaire measured at 12th week and after 3 months follow-up.
Time Frame
Baseline to 3 months "end of treatment"
Title
Adverse Events
Description
Adverse events documented by means of using open-ended questions at each contact.
Time Frame
Baseline to 3 months "end of treatment"
Title
Salivary cortisol
Description
Three samples of salivary cortisol (at awakening, 30 minutes after awakening, and at bedtime)were collected at baseline, after 12 weeks and 3 months after "end-of-treatment"
Time Frame
Baseline to 3 months after "end-of-treatment"

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: postmenopausal women (at least 12 months since last menstrual bleeding occurred or in previously hysterectomised women a serum follicle-stimulating hormone (S-FSH) defined as postmenopausal level according to references at the local laboratory) More or equal to 7 moderate to severe hot flashes or more or equal at 50 hot flashes per week according to a two-week screening diary ability to understand and speak Swedish freely given informed consent Exclusion Criteria: unstable thyroid or other metabolic disease treatment with hormone therapy (HT) or other complementary- or alternative treatments treatment for menopausal-related symptoms treatment with psychopharmacological drugs and/or sedatives d-un-treated psychiatric disease frequently exercising women (≥ 2h high-intensity activities/week)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth Nedstrand, Md, PhD
Organizational Affiliation
Ostergotland CC, University Hospital Dept. of Obstetrics and Gynecology, 582 85 Linköping, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital, Dept of Obstetrics and Gynecology
City
Linköping
ZIP/Postal Code
5851 85
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
10091202
Citation
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Results Reference
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15917156
Citation
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Results Reference
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PubMed Identifier
16390756
Citation
Nedstrand E, Wijma K, Wyon Y, Hammar M. Vasomotor symptoms decrease in women with breast cancer randomized to treatment with applied relaxation or electro-acupuncture: a preliminary study. Climacteric. 2005 Sep;8(3):243-50. doi: 10.1080/13697130500118050.
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PubMed Identifier
3318800
Citation
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Citation
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Applied Relaxation for Vasomotor Symptoms

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