- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02890628
Teenage Pregnancies in Refugee and Migrant Adolescents on the Thai-Myanmar Border
Perceptions and Experiences of Teenage Pregnancies in Refugee and Migrant Adolescents on the Thai-Myanmar Border
Study Overview
Status
Conditions
Detailed Description
The study will be conducted as follows:
- 12-24 individual interviews with pregnant or postnatal adolescent girls (<20 years);
- 1 Focus group discussion of 6-10 non-pregnant female adolescents (<20 years);
- 1 Focus group discussion of 6-10 adolescent men (<20 years);
- 1 Focus group discussion of 6-10 Shoklo malaria research unit antenatal care staff;
Interviews and focus group discussion will be conducted with study participants who agree to participate in discussions about teenage pregnancy and motherhood, sexual and reproductive health. In-depth interviews and focus group discussion will be conducted in private meeting rooms in proximity to the antenatal clinic waiting areas. In-depth interviews and Focus group discussion will be co-facilitated by the principal investigator and a trained counsellor/midwife fluent in Karen, Burmese and English. Focus group discussion will be run separately for Burmese- and Karen-speaking participants and participants will be separated by subgroup. Focus group discussion will include 6-10 participants per group and for each focus group discussion to last between 45-60 minutes. Individual in-depth interviews will last approximately 60 minutes each.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Tak
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Mae Sot, Tak, Thailand, 63110
- Shoklo Malaria Research Unit
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Inclusion criteria for adolescent mothers (subgroup 1) are:
- Aged 12 - <20 years
- Females
- Migrant or refugee status
- Myanmar nationality
- Any trimester of pregnancy or up to 12 month post partum
- Able and willing to participate and give informed consent
Inclusion criteria for non-pregnant female adolescents (subgroup 2) are:
- Aged <20 years
- Females
- Migrant or refugee status
- Myanmar nationality
- No past or current pregnancy
- Able and willing to participate and give informed consent
Inclusion criteria for adolescent men (subgroup 3) are:
- Aged <20 years
- Males
- Migrant or refugee status
- Myanmar nationality
- Able and willing to participate and give informed consent
Inclusion criteria for health staff (subgroup 4) are:
- No age restrictions
- Females or males
- Migrant, refugee or non-migrant status
- Any nationality
- Able and willing to participate and give informed consent
Exclusion Criteria:
- Any participant who is deemed by the researchers or health staff to be acutely physically or mentally unwell will be excluded.
- Participants who do not meet the age requirements, migration status or nationality requirements
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
pregnant/post-natal adolescents (<20 years)
12-24 individual with pregnant or postnatal adolescent girls (<20 years) will be interviewed.
|
|
non-pregnant female adolescents (<20 years)
1 Focus group discussion of 6-10 non-pregnant female adolescents (<20 years)
|
|
male adolescents (<20 year)
1 Focus group discussion of 6-10 adolescent men (<20 years)
|
|
SMRU health staff of antenatal clinics (ANC)
1 Focus group discussion of 6-10 Shoklo Malaria Research Unit antenatal clinic staff
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Thematic summary of adolescents' perceptions, experiences and beliefs in teenage pregnancy, motherhood, sexual and reproductive health, family planning and support structures adolescent refugees and migrants
Time Frame: up to 1 year
|
up to 1 year
|
|
Descriptive summary of demographic, social and medical characteristics of study participants
Time Frame: up to 1 year
|
up to 1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Summary of antenatal clinic staff perceptions
Time Frame: up to 1 year
|
up to 1 year
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SMRU 1602
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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