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Effect of Short-Term Preoperative Yoga on Breathing and Recovery in Women Undergoing Robotic Gynecological Surgery

Immediate preoperative yoga based interventions and risk stratification to enhance recovery and outcomes in robotic gynecological surgery An open labelled double arm pilot randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094587
Enrollment
60
Registered
2025-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: N70-N77- Inflammatory diseases of female pelvic organs Health Condition 2: N80-N98- Noninflammatory disorders of female genital tract

Interventions

Intervention1: Yoga Based Intervention: Timing: 3 days prior to 2 weeks post surgery, twice daily, 30 minutes/session Techniques: Pranayama, Guided Relaxation, Gentle Movements, Bedside or video-guid

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female patients, age 18 65 years Elective robotic gynecological surgeries ASA Grade I and II Informed consent

Exclusion criteria

Exclusion criteria: 1. Patient unwillingness or any contraindications to yoga practices like severe respiratory or cardiovascular issues 2. Patients with a history of recent respiratory tract infections or pneumonia within the last two weeks 3. Emergency surgical cases or patients unable to undergo preoperative yoga due to scheduling limitations 4. BMI more than or equal to 30 5. Regular yoga practitioner or athlete. 6. Patients with a history of cognitive impairment or psychiatric disorders that may affect their ability to participate in the study

Design outcomes

Primary

MeasureTime frame
Perioperative Respiratory Parameters (FVC, tidal volume, respiratory rate) via Wright RespirometerTimepoint: Before starting of intervention, in preoperative room, 24hours postoperatively and after 2weeks post operatively.

Secondary

MeasureTime frame
Anxiety by STAITimepoint: pre intervention and in preoperative room;Postoperative pain by NRSTimepoint: 6, 12, 24 hr post operatively;Analgesic consumptionTimepoint: first 48h;Time to ambulation Timepoint: started walking first time postoperatively;Return of bowel functionTimepoint: Flatus or faeces passing first time post operatively;Hospital discharge timeTimepoint: days to discharge;Wound healing (suture removal)Timepoint: time to suture removal;Nutrition (NRI, BMI, Serum albumin, Hemoglobin)Timepoint: Pre intervention, 24 hr postoperative and 2 weeks postoperatively;Inflammatory markers NLRTimepoint: Pre intervention, 24 hr postoperative and 2 weeks postoperatively

Countries

India

Contacts

Public ContactDr Yashwant Singh Payal

All India Institute of Medical Sciences, Rishikesh

dryspayal05@gmail.com9411789762

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026