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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05386706
Other study ID # Digital Intervention PCOS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 21, 2022
Est. completion date September 1, 2023

Study information

Verified date November 2023
Source Shanghai 10th People's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

With the change in environment and lifestyle, and the improvement of people's understanding of PCOS, the incidence of PCOS is increasing worldwide. According to statistics, the prevalence of PCOS in premenopausal women is as high as 5-20%. Lifestyle interventions are the main treatment option for patients with PCOS. In addition, research has shown that digital therapy can effectively improve behavior changes in diet, exercise, and medication adherence, predict disease progression, reduce the frequency of disease-related symptoms, and promote effective disease management. This study aimed to investigate the efficacy of digital intervention versus traditional metformin monotherapy in patients with PCOS.


Description:

This study developed a mini-program that combined diet, exercise, sleep, and mood interventions for PCOS women.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date September 1, 2023
Est. primary completion date August 12, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: Female aged 18- 45; Meet Rotterdam criteria; Insulin Resistance Exclusion Criteria: Women who are pregnant or have a pregnancy plan within six months; Congenital adrenocortical hyperplasia; Hyperprolactinemia; Hyperthyroidism or hypothyroidism; Abnormal liver function (= 3 times the upper limit of the normal range); Abnormal renal function (GFR<60ml/min/1.73m2); Adrenal or ovarian tumors secreting androgens; Used contraceptives, metformin, pioglitazone, and antidepressant medication in the last 3 months.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Digital Intervention
This study developed a mini-program that combined diet, exercise, sleep, and mood interventions for PCOS women.
Drug:
Metformin
Traditional metformin monotherapy.

Locations

Country Name City State
China Department of Endocrinology, Shanghai Tenth People's Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai 10th People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Homeostasis model assessment of insulin resistance insulin resistance index 3 months
Secondary Anthropometry body mass index (kg/m2) 3 months
Secondary menstrual frequency number of menstruation in a year 3 months
Secondary fasting glucose fasting glucose(mmol/L) 3 months
Secondary fasting insulin fasting insulin(mmol/L) 3 months
Secondary Total cholesterol Total cholesterol (mmol/L) 3 months
Secondary Triglycerides Triglycerides (mmol/L) 3 months
Secondary HDL-c HDL-c (mmol/L) 3 months
Secondary LDL-c LDL-c (mmol/L) 3 months
Secondary total testosterone total testosterone (nmol/L) 3 months
Secondary free testosterone free testosterone (nmol/L) 3 months
Secondary Sex hormone-binding globulin Sex hormone-binding globulin (nmol/L) 3 months
Secondary Androstenedione Androstenedione (ng/ml) 3 months
Secondary Dehydroepiandrosterone Dehydroepiandrosterone (ug/dl) 3 months
Secondary International Physical Activity Questionnaire (IPAQ) Assess physical activity situation in women with PCOS. 3 months
Secondary Pittsburgh Sleep Quality Index (PSQI) Assess sleep situation in women with PCOS. 3 months
Secondary Hospital Anxiety and Depression Scale (HADS) To evaluate anxiety and depression in PCOS women. 3 months
Secondary Three-Factor Eating Questionnaire (TFEQ-R21) Assess eating behavior in women with PCOS. 3 months
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