Polycystic Ovary Syndrome Clinical Trial
— IPAPOfficial title:
Interpersonal Psychotherapy in Adolescents With Polycystic Ovary Syndrome
Verified date | September 2023 |
Source | University of Colorado, Denver |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of this study is to find out whether taking part in a group-based interpersonal psychotherapy (IPT) program designed to improve mood and lessen stress in girls with PCOS will improve depression, unhealthy eating behaviors, weight, and insulin resistance.
Status | Completed |
Enrollment | 30 |
Est. completion date | July 14, 2023 |
Est. primary completion date | July 14, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 12 Years to 17 Years |
Eligibility | Inclusion Criteria: - Diagnosed with PCOS duration > 3 months - 12-17 years old - BMI > 75th percentile - CESD > 16 Exclusion Criteria: - Weekly or bi-weekly therapy with licensed behavioral health provider - Inability to speak, read, or write in English (teen) - Major medical conditions - HbA1c > 7.0% - Hormonal contraception < 3 months - Metformin < 3 months - Antidepressants/psychotropic medications < 4 weeks |
Country | Name | City | State |
---|---|---|---|
United States | Children's Hospital Colorado | Aurora | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Denver | American Psychological Association (APA) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Center for Epidemiologic Studies-Depression Scale | Depression symptoms will be assessed by the Center for Epidemiologic Studies-Depression Scale. Scores range from 1 to 4. The scoring of positive items is reversed. Possible range of scores is zero to 60, with the higher scores indicating the presence of more symptomatology. | Baseline | |
Primary | Center for Epidemiologic Studies-Depression Scale | Depression symptoms will be assessed by the Center for Epidemiologic Studies-Depression Scale. Scores range from 1 to 4. The scoring of positive items is reversed. Possible range of scores is zero to 60, with the higher scores indicating the presence of more symptomatology. | 6-Week Follow-Up Assessment | |
Primary | Center for Epidemiologic Studies-Depression Scale | Depression symptoms will be assessed by the Center for Epidemiologic Studies-Depression Scale. Scores range from 1 to 4. The scoring of positive items is reversed. Possible range of scores is zero to 60, with the higher scores indicating the presence of more symptomatology. | 6-Month Follow-Up Assessment | |
Secondary | Emotional Eating Scale Adapted for Children | Disordered eating will be assessed by the Emotional Eating Scale Adapted for Children. The scale has been adapted for children and assesses eating in response to negative affect, such as feeling sad or irritated. The scale ranges from "I have no desire to eat" to "I have a very strong desire to eat" and averages how many days a week the participant eats based on that feeling. | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment | |
Secondary | Loss-of-Control Eating Disorder Questionnaire | Loss-of-control eating will be assessed via the 19-item Loss-of-Control Eating Disorder Questionnaire (LOC-ED-Q), which shows sound psychometric properties in adolescents using Yes/No. | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment | |
Secondary | Reward Based Eating Drive Scale | Reward based eating will be assessed by the Reward Based Eating Drive Scale. This is a self-report questionnaire which assesses reward-based eating that shows sound psychometric properties. The total score is summed at the end; a higher total is indicative of reward-based eating. | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment | |
Secondary | BMI | Fasting BMI (kg/m2) will be derived from measured height in triplicate by stadiometer and measured fasting weight by calibrated digital scale. BMI z-score and BMI %ile will be computed to determine eligibility (BMI =75th percentile). | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment | |
Secondary | Insulin Resistance | Blood will be sampled via a venipuncture procedure following a 10-hour overnight fast to measure fasting insulin. Insulin resistance will be estimated from fasting insulin and glucose with the homeostatic model assessment of insulin resistance (HOMA-IR). | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment | |
Secondary | Dysglycemia | Blood will be sampled via a venipuncture procedure following a 10-hour overnight fast to measure fasting insulin. Insulin resistance will be estimated from fasting insulin and glucose with the homeostatic model assessment of insulin resistance (HOMA-IR). | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment | |
Secondary | Dyslipidemia | Blood will be sampled via a venipuncture procedure following a 10-hour overnight fast to measure dyslipidemia. Insulin resistance will be estimated from fasting insulin and glucose with the homeostatic model assessment of insulin resistance (HOMA-IR). | Baseline, 6-Week Follow-Up Assessment, 6-Month Follow-Up Assessment |
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