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Effectiveness of face to face physiotherapy training and education for women who are undergoing elective Cesarean section in minimizing the post-operative complications following Cesarean section. A Randomized controlled trial

Effectiveness of face to face physiotherapy training and education for women who are undergoing elective Cesarean section. A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2019/029
Enrollment
Unknown
Registered
2019-09-06
Start date
2019-09-06
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

Complications following elective Cesarean Section

Interventions

*Study setting - De Soysa Maternity Hospital for Women, Colombo *Randomization method and procedure - Participants will be randomly assigned in to two groups as intervention group and control group,

Sponsors

BSc. Physiotherapy Degree Programme, Department of Allied Health Sciences, Faculty of Medicine, University of Colombo.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age between 20 – 40 years • Women who undergo Uncomplicated Category ‘4’ Cesarean delivery under spinal anesthesia, due to obstetric indications such as repeat cesarean delivery, pelvic abnormalities that preclude engagement, malpresentation of fetus, dystocia and elective CS. • Patients who are discharged on the post-operative day 3

Exclusion criteria

Exclusion criteria: * Patients who have undergone two or several C sections or abdominal surgeries previously . * Patients who have complicated obstetric problems such as Diabetes Mellitus, Systemic Lupus Erythematosus, connective tissue disorders. * Patients on maternal sepsis. * Patients on Disease Modifying Anti Rheumatic Drugs (DMARDs) and oral steroids. * Patients who cannot be given with physiotherapy interventions. * Mentally ill patients. * Patients who are in the Intensive Care Unit (ICU). * Deliveries with post-operative complications. * C- sections with general/ epidural anesthesia and using patient controlled anesthesia. * Patients with abdominal hernia. * Patients with DRA (Diastasis Rectus abdominis) larger than 2cm.

Design outcomes

Primary

MeasureTime frame
The post-operative pain score using the VAS (Visual Analogue Scale for pain assessment). [On the day of discharge. Day 3 of the CS] Additional requirement of analgesics for the pain relief (apart from routine standard protocol) using the medical records. On the day of discharge [On the day of discharge. Day 3 of the CS] The length of hospital stay using the medical records. On the day of discharge [On the day of discharge. Day 3 of the CS] [] [] [ ] [] [ ] [ ] [] [] [] [] [ ] [] [] [ ] [] [ ] [ ] [] [] [ ] [ ] [ ] [ ] [ ] [] [] [] [] [] [ ] [ ] [ ] [ ] [ ] [ ] [ ] [] [ ] [] [ ] [] [] [ ] [ ] [] [] [] [ ] [ ] [ ] [] [] [] [ ] [ ] [ ] [ ] [] [] [] [ ] [] [ ] [] [] [] [] [] [] [] [] [] [ ] [ ] [] [ ] [] [ ] [ ] [] [ ]

Secondary

MeasureTime frame
Quality of post-natal life of both groups using Short Form Health Survey tool (SF-36)- Self-administered questionnaire. [After 6 weeks of the Cesarian Section.]

Countries

Sri Lanka

Contacts

Public ContactKalani Weerasinghe

University student

kalani.weerasingha549@gmail.com0112695300 ext 240

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 9, 2026