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A randomized controlled trial to evaluate the effectiveness of an ehealth antenatal exercise intervention in improving lumbopelvic pain in Hong Kong chinese pregnant women

A randomized controlled trial to evaluate the effectiveness of an ehealth antenatal exercise intervention in improving lumbopelvic pain in Hong Kong chinese pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011308
Enrollment
Unknown
Registered
2017-05-04
Start date
2017-05-15
Completion date
Unknown
Last updated
2017-05-09

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

Conditions

lumbopelvic pain

Interventions

Two groups:usual antenatal care and antenatal exercise intervention versus Usual antenatal care

Sponsors

The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. healthy Hong Kong Chinese pregnant women; 2. aged 18–45 years; 3. from 13th to 24th weeks gestation; 4. who can read, write, and speak Chinese; 5. who possess a smartphone.

Exclusion criteria

Exclusion criteria: 1. contraindication against performing antenatal exercise as listed by the American College of Obstetricians and Gynecologist (2015); 2. any current or past history of psychiatric disease; 3. refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
the prevalence of LPP;functional disability of LPP;—

Secondary

MeasureTime frame
physical activity level;risk of antenatal depression;—

Countries

China

Contacts

Public ContactAu Yeung Elce

The Chinese University of Hong Kong

ae483@ha.org.hk+852 35053713

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026