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A Quasi Experiment study to evaluate the effectiveness of a combined prenatal yoga and peer group support intervention in reducing anxiety and salivary cortisol levels in pregnant women

A Quasi Experiment study to evaluate the effectiveness of a combined prenatal yoga and peer group support intervention in reducing anxiety and salivary cortisol levels in pregnant women

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251125006
Enrollment
124
Registered
2025-11-25
Start date
2025-11-28
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Prenatal anxiety and elevated cortisol levels in pregnant women Prenatal anxiety Pregnant women Cortisol level Prenatal yoga Peer group support Quasi experimental study Maternal mental health

Interventions

Pregnant women in the intervention group will participate in a combined program of prenatal yoga and peer group support for 8 weeks. Prenatal yoga sessions (60 minutes each) are conducted twice a week
Experimental Behavioral,Experimental Behavioral
Combined Prenatal Yoga and Peer Group Support,Standar Antenatal Care

Sponsors

Beasiswa Pendidikan Indonesia Kementerian Pendidikan, Kebudayaan, Riset, dan Teknologi (BPI Kemendikbudristek)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Gestational age between 22 and 32 weeks 2. Either primigravida or multigravida 3. Experiencing moderate to high anxiety levels assessed using the State Trait Anxiety Inventory. 4. Able to join yoga and peer support sessions. 5. Willing to give informed consent.

Exclusion criteria

Exclusion criteria: 1. Women with obstetric complications or medical contraindications to exercise, 2. Using psychiatric medication or receiving psychological therapy. 3. With chronic medical conditions such as hypertension or diabetes, and those unable to attend the intervention sessions regularly.

Design outcomes

Primary

MeasureTime frame
Anxiety level Baseline (pre-intervention) and after 6 weeks of intervention (post-intervention). Measured using the State-Trait Anxiety Inventory (STAI), a standardized questionnaire assessing both state and trait anxiety levels in pregnant women.

Secondary

MeasureTime frame
cortisol hormone level Baseline (pre-intervention) and after 6 weeks of intervention (post-intervention). Measured from saliva samples using Enzyme-Linked Immunosorbent Assay (ELISA) method to determine cortisol concentration.

Countries

Indonesia

Contacts

Public ContactKenik Wahyuni

Universitas Diponegoro

keniksriwahyuni@respati.ac.id085869722077

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026