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Breathing Exercises on Depression in Postmenopausal Women

Effect of Breathing Exercises on Depression and Sexual Function in Postmenopausal Women

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06741384
Enrollment
60
Registered
2024-12-19
Start date
2024-12-26
Completion date
2025-03-25
Last updated
2024-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postmenopausal, Depressive Symptom, Breathing Exercises

Brief summary

Evaluate the effect of breathing exercises on depression and sexual function in postmenopausal women

Detailed description

Sixty postmenopausal women will be sourced from the Obstetrics & Gynecology outpatient clinic at El Mahalla El Kobra general hospital in Egypt, with referrals from gynecologists. Patients will be randomly assigned into two groups. Study group: It will include 30 women participating in diaphragmatic breathing plus aerobic training. Control group: It will include 30 women participating in aerobic training. At baseline and poststudy, the following outcomes will be assessed: 1. Depression (Beck Depression Inventory II scale). 2. Sexual function (female sexual function index questionnaire).

Interventions

Participants will be directed to position their hands on the rectus abdominis muscle located under the anterior chest wall while resting in a hook position. They will be instructed to inhale slowly and deeply via the nostrils, expanding their abdomen without raising their upper chest, and resting their shoulders. Following the cessation of respiration, the woman will slowly exhale by pursing her lips. A respiratory cycle will consist of a three-second inhalation, a three-second pause, and a six-second exhalation. The diaphragmatic training regimen will consist of doing 3-5 sets of 5-10 deep breaths, with 2-minute intervals of rest in between sets.

OTHERAerobic training

The women will participate in aerobic training on cycle ergometer. Each session will consist of 30-45 minutes of cycling at a moderate intensity, accompanied by a workout heart rate ranging from 65% to 75% of the maximal heart rate and ranging between 12 and 14 on the Borg rating of perceived exertion 20-point scale. After ten minutes of warm-up, every session will end with a brief 3-minute period of cool-down.

Sponsors

Middle East University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Minimum of 3 years after menopause. * Mild to moderate depression. * Mild to moderate sexual dysfunction. * Their ages will be ranged from 45 to 60 years old. * Their BMI will be less than 30 kg/m2.

Exclusion criteria

* Prolapse of the pelvic organs. * Pelvic tumors. * Vaginal infections. * Musculoskeletal/ neurological limitations to exercise. * Psychiatric disorders. * Unstable cardiovascular conditions. * Diabetes.

Design outcomes

Primary

MeasureTime frameDescription
DepressionAt baseline and after 8 weeksThe second edition of Beck depression inventory scale will be scored. The second edition of Beck depression inventory scale consists of 21- items. Item scores ranging from 0 to 3 are combined to produce a total score that ranges from 0 to 63 using the cumulative scoring technique. Elevated scores suggest a more severe level of depression.

Secondary

MeasureTime frameDescription
Sexual functionAt baseline and after 8 weeksFemale sexual function index questionnaire will be scored. The female sexual function index questionnaire is a 19-item, self-report measure of female sexual function that provides scores on overall levels of sexual function. The 19 items of the female sexual function index questionnaire use a 5-point scale ranging from 1 to 5 with higher scores indicating greater levels of sexual functioning on the respective item. Total scores of 26.5 or lower characterize sexual dysfunction.

Contacts

Primary ContactSaher Elgayar, Ph.D
saherlotfy020@gmail.com01020429911
Backup ContactMohammed Elhamrawy, Ph.D

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026