Cognitive Behavioral Group Therapy for the Management of Menopause Symptoms in Mood Disorders



Status:Completed
Conditions:Depression, Depression, Major Depression Disorder (MDD), Psychiatric, Women's Studies, Bipolar Disorder
Therapuetic Areas:Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Reproductive
Healthy:No
Age Range:40 - 65
Updated:11/11/2018
Start Date:July 2016
End Date:October 2018

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Cross-Cultural Cognitive Behavioral Group Therapy: Evaluating the Effectiveness of a Manualized Cognitive Behavior Group Therapy Treatment for the Management of Menopause Symptoms in a Mood and Anxiety Disorder Population

The general objective of this study is to advance insight into non-pharmacological treatments
for maturing women that impact psychological health and wellbeing of women adapting to
menopause, a natural but often challenging developmental milestone.

This exploratory study proposes to expand the knowledge in the menopausal literature and
evaluate the effectiveness of cognitive-behavioral group therapy (CBGT) in reducing
problematic vasomotor symptoms, reducing daily interference and improving quality of life.
The study will include two homogenous peri- or post-menopausal cohorts (African-American and
Caucasian) with major depressive disorder or bipolar disorder. The intervention will be
delivered in groups of 6 to 10 participants per group of both race/ethnicities in an
outpatient setting during a 6-week time period. The participants will be assessed on the
degree of hot flash problem rating, hot flash related daily interference, and menopause
quality of life at screening, baseline, and post-treatment. Participants will also be
assessed using the following predictor variables at the same time points: body mass index
(BMI), level of perceived stress, severity of depression, severity of anxiety level of
pleasure, severity of mania, hot flash beliefs and severity of couple's conflict.

Inclusion Criteria.

1. Self-identified as African-American or Caucasian females between 40-65 experiencing
the early, late peri-menopause or early or late post-menopause stages of reproductive
aging defined by The North American Menopause Society (NAMS, 2014), Menopause Practice
guidelines, stages of reproductive aging. There are situations in which menopause
status will not be able to be determined, such as with women who have had a
hysterectomy. However, if the potential study participant meets all other inclusion
criteria, then she can be enrolled in the study.

2. Diagnosed with current or lifetime bipolar disorder or major depressive disorder as
assessed by the MINI International Neuropsychiatric Interview (MINI) for Diagnostic
and Statistical Manual-5 (DSM-5).

3. Menopause symptoms can be natural or surgically induced.

4. Willing to remain on current dose of psychotropic medications until the study has
concluded.

5. Experiencing one or more hot flashes and/or night sweats per day.

6. Willing to have the 6 CBGT interventions audio recorded.

7. English speaking with at least a high school education.

8. Montgomery-Asberg Depression Rating Scale (MADRS) total score > 7

9. Women stable on psychotropic medications for ≥ 8 weeks.

Medication regimens to treat their DSM-V diagnoses will be encouraged to continue in order
to determine if the CBGT accounted for any change in symptoms.

Exclusion Criteria.

1. Unwilling or unable to comply to study requirements.

2. Women diagnosed with schizophrenia, schizoaffective, borderline personality disorder,
and/or active psychosis, as confirmed by MINI.

3. Diagnosed with active substance use disorder within past 12 months as confirmed on the
MINI.

4. Women currently treated with hormone therapy (HT) for Vasomotor Symptoms (VMS).

5. Diagnosed with current post-traumatic stress disorder (PTSD).

6. Participants experiencing acute mania as defined by a Young Mania Rating Scale (YMRS)
score > 15

7. Serious suicidal risks judged by the investigator or having score equal or greater
than 4 on MADRS item number 10 at screening or baseline.

8. Participants being treated with chemotherapy and/or tamoxifen.

9. Women who are not self-identifying as either African-American or Caucasian.
We found this trial at
1
site
Cleveland, Ohio 44106
Principal Investigator: Danette Conklin, PhD
Phone: 216-844-2862
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mi
from
Cleveland, OH
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