Effect of Group Education and Individual Counselling on Mental Health and Quality of Life in 45-60 Year Old Women

June 19, 2023 updated by: Vastra Gotaland Region

The Effect of Group and Individual Counseling on Mental Health, Quality of Life and Sick Leave in 45-60 Year Old Women With Stress Related Symptoms - A Randomized Controlled Trial

Background:

Stress-related ill health is today the most common cause of long-term sick leave in women in the middle of life and a common cause of visits to primary health care.

Objective:

To implement and investigate the effect of education in group and/or individually held in primary health care clinics embracing aspects of mental health, quality of life, sick leave and the needs women aged 45-60 with stress-related symptoms have.

Method The study is a randomized controlled trial with a two-factor design. The study evaluates both group information (GI) and structured person-centered support (PCS) and possible interaction effects between these two treatment modalities. The group education consists of four information sessions discussing myths around menopause, physiology, local estrogen deficiency symptoms, women's cardiovascular health, stress-related ill health, mental health, relationships, sexuality, lust and possible treatment options. In addition, conversations about insight into obstacles and resources, coping strategies and behavioral changes will be included. The individually structured person-centered support comprises of five meetings consisting of dialogue on symptoms of stress-related ill health, physiology and coping strategies. Participants will be block randomized into four groups; GI, PCS, GI+PCS or control.

Expected result Implementation of group and individual support calls is expected to improve health for women seeking primary care care. The results are expected to increase the knowledge of how women's health is affected by short-term care in primary care through reduced sick leave days, reduced care needs, return to work and increased quality of life. The result may improve existing primary care routines for women, and if needed, for a more individualized care contact and support.

Study Overview

Detailed Description

Background:

Stress-related ill health is today the most common cause of long-term sick leave in women in the middle of life and a common cause of visits to primary health care. Women seem to suffer more than men in the same age group. Few evidence based treatment options exist and none of them has a proven effect on return to work.

Objective:

To implement and investigate the effect of education in group and/or individually held in primary health care clinics embracing aspects of mental health, quality of life, sick leave and the needs women aged 45-60 with stress-related symptoms have.

Method The study is a randomized controlled trial with a two-factor design. The study evaluates both group information (GI) and structured person-centered support (PCS) and possible interaction effects between these two treatment modalities. The group education consists of four information sessions discussing myths around menopause, physiology, local estrogen deficiency symptoms, women's cardiovascular health, stress-related ill health, mental health, relationships, sexuality, lust and possible treatment options. In addition, conversations about insight into obstacles and resources, coping strategies and behavioral changes will be included. The individually structured person-centered support comprises of five meetings consisting of dialogue on symptoms of stress-related ill health, physiology and coping strategies. Participants will be block randomized into four groups; GI, PCS, GI+PCS or control.

Expected result Implementation of group and individual support calls is expected to improve health for women seeking primary care care. The results are expected to increase the knowledge of how women's health is affected by short-term care in primary care through reduced sick leave days, reduced care needs, return to work and increased quality of life. The result may improve existing primary care routines for women, and if needed, for a more individualized care contact and support.

Study Type

Interventional

Enrollment (Actual)

370

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Vastra Gotaland
      • Boras, Vastra Gotaland, Sweden, 503 38
        • Research and Development Unit

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • The woman has at least one possible stress related problem such as depression, anxiety, gastrointestinal disturbance, unexplained muscular pain or cardiovascular illness such as hypertension or coronary heart disease.
  • The woman have not been on sick leave for more than 30 days during the preceding 60 days.
  • The woman can easily understand and communicate freely in the Swedish language.
  • The woman does not have severe mental illness such as schizophrenia, other psychosis or known neuropsychiatric disorder. The woman is not in terminal palliative care.
  • The woman does not have severe depression (MADRS scores >20 or express suicidal ideation)

Exclusion Criteria:

  • The woman do not wish to continue participation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1
This group will receive the intervention Group information (GI).
The group education consists of four information sessions discussing myths and myths around menopause, physiology, local estrogen deficiency symptoms, women's cardiovascular health, stress-related ill health, mental health, relationships, sexuality, lust and possible treatment options. In addition, conversations about insight into obstacles and resources, coping strategies and behavioral changes will be included.
Experimental: Group 2
This group will receive the intervention Group information (GI) followed by Structured person-centered support (PCS)
The group education consists of four information sessions discussing myths and myths around menopause, physiology, local estrogen deficiency symptoms, women's cardiovascular health, stress-related ill health, mental health, relationships, sexuality, lust and possible treatment options. In addition, conversations about insight into obstacles and resources, coping strategies and behavioral changes will be included.
The individually structured person-centered support comprises of five meetings consisting of dialogue on symptoms of stress-related ill health, physiology and coping strategies.
Experimental: Group 3
This group will receive the intervention Structured person-centered support (PCS)
The individually structured person-centered support comprises of five meetings consisting of dialogue on symptoms of stress-related ill health, physiology and coping strategies.
No Intervention: Group 4
This is a control group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short term effect of group education (GI) on change in quality of life
Time Frame: Change from baseline to six months after completed intervention
What is the effect of group education (GI) on quality of life (measured by change in scores in SF36 from baseline to 6 months after completed intervention)
Change from baseline to six months after completed intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Short term effect of Structured person-centered support (PCS) on change in days on sick leave
Time Frame: Change from baseline to six months after completed intervention
What is the effect of Structured person-centered support (PCS) on change in number of days on sick leave. (At baseline the number of days on sick leave up until present time is stated by women currently being on sick leave. At the 6 month follow the same information is retrieved is retrieved. The change is the difference between these measurements.)
Change from baseline to six months after completed intervention
Short term effect of Structured person-centered support (PCS) on change in depressive mood
Time Frame: Change from baseline to six months after completed intervention
What is the effect of Structured person-centered support (PCS) on depressive mood (measured by change in scores in MADRS from baseline to 6 months after completed intervention)
Change from baseline to six months after completed intervention
Short term effect of Structured person-centered support (PCS) on change in quality of life
Time Frame: Change from baseline to six months after completed intervention
What is the effect of Structured person-centered support (PCS) on quality of life (measured by change in scores in SF36 from baseline to 6 months after completed intervention)
Change from baseline to six months after completed intervention
Short term effect of Structured person-centered support (PCS) on stress levels
Time Frame: Change from baseline to six months after completed intervention
What is the effect of Structured person-centered support (PCS) on stress levels (measured by change in scores in PSS-14 from baseline to 6 months after completed intervention)
Change from baseline to six months after completed intervention
Short term effect of group education (GI) on change in days on sick leave
Time Frame: Change from baseline to six months after completed intervention
What is the effect of group education (GI) on change in number of days on sick leave. (At baseline the number of days on sick leave up until present time is stated by women currently being on sick leave. At the 6 month follow the same information is retrieved is retrieved. The change is the difference between these measurements.)
Change from baseline to six months after completed intervention
Short term effect of group education (GI) on change in depressive mood
Time Frame: Change from baseline to six months after completed intervention
What is the effect of group education (GI) on depressive mood (measured by change in scores in MADRS from baseline to 6 months after completed intervention)
Change from baseline to six months after completed intervention
Short term effect of group education (GI) on stress levels
Time Frame: Change from baseline to six months after completed intervention
What is the effect of group education (GI) on stress levels (measured by change in scores in PSS-14 from baseline to 6 months after completed intervention).
Change from baseline to six months after completed intervention
Long term effect of Structured person-centered support (PCS) on change in days on sick leave
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of Structured person-centered support (PCS) on change in number of days on sick leave. (At baseline the number of days on sick leave up until present time is stated by women currently being on sick leave. At the 12 month follow the same information is retrieved is retrieved. The change is the difference between these measurements.)
Change from baseline to 12 months after completed intervention
Long term effect of Structured person-centered support (PCS) on change in depressive mood
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of Structured person-centered support (PCS) on depressive mood (measured by change in scores in MADRS from baseline to 12 months after completed intervention)
Change from baseline to 12 months after completed intervention
Long term effect of Structured person-centered support (PCS) on change in quality of life
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of Structured person-centered support (PCS) on quality of life (measured by change in scores in SF36 from baseline to 12 months after completed intervention)
Change from baseline to 12 months after completed intervention
Long term effect of Structured person-centered support (PCS) on stress levels
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of Structured person-centered support (PCS) on stress levels (measured by change in scores in PSS-14 from baseline to 12 months after completed intervention)
Change from baseline to 12 months after completed intervention
Long term effect of group education (GI) on change in days on sick leave
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of group education (GI) on change in number of days on sick leave. (At baseline the number of days on sick leave up until present time is stated by women currently being on sick leave. At the 12 month follow the same information is retrieved is retrieved. The change is the difference between these measurements.)
Change from baseline to 12 months after completed intervention
Long term effect of group education (GI) on change in depressive mood
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of group education (GI) on depressive mood (measured by change in scores in MADRS from baseline to 12 months after completed intervention)
Change from baseline to 12 months after completed intervention
Long term effect of group education (GI) on change in quality of life
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of group education (GI) on quality of life (measured by change in scores in SF36 from baseline to 12 months after completed intervention)
Change from baseline to 12 months after completed intervention
Long term effect of group education (GI) on stress levels
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of group education (GI) on stress levels (measured by change in scores in PSS-14 from baseline to 12 months after completed intervention).
Change from baseline to 12 months after completed intervention
Short term effect of group education (GI) on levels of anxiety
Time Frame: Change from baseline to 6 months after completed intervention
What is the effect of group education (GI) on stress levels (measured by change in scores in HAD from baseline to 6 months after completed intervention).
Change from baseline to 6 months after completed intervention
Long term effect of group education (GI) on levels of anxiety
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of group education (GI) on stress levels (measured by change in scores in HAD from baseline to 12 months after completed intervention).
Change from baseline to 12 months after completed intervention
Short term effect of Structured person-centered support (PCS) on levels of anxiety
Time Frame: Change from baseline to 6 months after completed intervention
What is the effect of Structured person-centered support (PCS) on stress levels (measured by change in scores in HAD from baseline to 6 months after completed intervention).
Change from baseline to 6 months after completed intervention
Long term effect of Structured person-centered support (PCS) on levels of anxiety
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of Structured person-centered support (PCS) on stress levels (measured by change in scores in HAD from baseline to 12 months after completed intervention).
Change from baseline to 12 months after completed intervention
Short term effect of Structured person-centered support (PCS) on visits to primary health care
Time Frame: Change from baseline to 6 months after completed intervention
What is the effect of Structured person-centered support (PCS) on visits to primary health care (women are asked at baseline if they had to visit the primary health care center during the preceding two months. The same question is asked at 6 months. The measurement is the change in proportion of women who visited the primary health care center).
Change from baseline to 6 months after completed intervention
Long term effect of Structured person-centered support (PCS) on visits to primary health care
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of Structured person-centered support (PCS) on visits to primary health care (women are asked at baseline if they had to visit the primary health care center during the preceding two months. The same question is asked at 12 months. The measurement is the change in proportion of women who visited the primary health care center).
Change from baseline to 12 months after completed intervention
Short term effect of group education (GI) on visits to primary health care
Time Frame: Change from baseline to 6 months after completed intervention
What is the effect of group education (GI) on visits to primary health care (women are asked at baseline if they had to visit the primary health care center during the preceding two months. The same question is asked at 6 months. The measurement is the change in proportion of women who visited the primary health care center).
Change from baseline to 6 months after completed intervention
Long term effect of group education (GI) on visits to primary health care
Time Frame: Change from baseline to 12 months after completed intervention
What is the effect of group education (GI) on visits to primary health care (women are asked at baseline if they had to visit the primary health care center during the preceding two months. The same question is asked at 12 months. The measurement is the change in proportion of women who visited the primary health care center).
Change from baseline to 12 months after completed intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Lena Rindner, Vastra Gotaland region, Sweden

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 24, 2018

Primary Completion (Actual)

February 26, 2020

Study Completion (Actual)

November 6, 2020

Study Registration Dates

First Submitted

August 29, 2018

First Submitted That Met QC Criteria

September 5, 2018

First Posted (Actual)

September 10, 2018

Study Record Updates

Last Update Posted (Actual)

June 22, 2023

Last Update Submitted That Met QC Criteria

June 19, 2023

Last Verified

November 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • U1111-1219-6542

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The descriptive data provided will be summary data for each group. The investigators will not show data from single participants.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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