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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06015919
Other study ID # P.T.REC/012/003872
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 5, 2022
Est. completion date August 20, 2023

Study information

Verified date August 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A study of effect of dash diet and acupuncture on hypertension in postmenopausal women


Description:

45 of post menopausal women divided into three groups A,B,C - Group (A): It will include 15 post-menopausal women who will be treated by DASH diet and anti-hypertensive drugs. - Group (B): It will include 15 post-menopausal women who will be treated by acupuncture and anti-hypertensive drugs. - Group (C): It will include 15 post-menopausal women who will be treated by DASH diet, acupuncture and anti-hypertensive drugs.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date August 20, 2023
Est. primary completion date April 25, 2023
Accepts healthy volunteers No
Gender Female
Age group 50 Years to 60 Years
Eligibility Inclusion Criteria: - Their body mass index will be ranged from 25 -29.9 kg/m2 - All patients will be medically stable when attending the study. - The DASH eating plan of 1800 kcal per day will be used in the study. Exclusion Criteria: - Auditory and visual problems. - Chronic renal failure. - Myocardial infarction or arrythmias with heart failure.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
dash diet
Group (A): It will include 15 post-menopausal women who will be treated by DASH diet and anti-hypertensive drugs. Group (B): It will include 15 post-menopausal women who will be treated by acupuncture and anti-hypertensive drugs. Group (C): It will include 15 post-menopausal women who will be treated by DASH diet, acupuncture and anti-hypertensive drugs.
Device:
Acupuncture
acupuncture

Locations

Country Name City State
Egypt Alaa Nabil Elsayed Mohamed Abu hammad Elsharqia

Sponsors (2)

Lead Sponsor Collaborator
Cairo University faculty of physical therapy

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other assessment of quality of life it will be measured by sf 36 questionnaire pre and post treatment 3 months
Primary blood pressure it will be measured by sphygmomanometer pre and post treatment 3 months
Secondary sodium and potassium levels it will be measured by blood analysis pre and post treatment 3 months
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