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Effect of a preoperative nutritional education video on quality of life in patients undergoing gynecologic surgery : A Randomized Controlled Trial

Efficacy of a Video-Based Preoperative Nutritional Education Intervention on Postoperative Quality of Life Among Patients Undergoing Gynecologic Surgery: A Randomized Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260422002
Enrollment
250
Registered
2026-04-22
Start date
2026-04-07
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

Primary: Postoperative quality of life in patients undergoing gynecologic surgery Secondary: Nutritional status Malnutrition risk Postoperative complications Length of hospital stay Gynecologic surgery Preoperative care Nutritional education Video based intervention Quality of life EQ5D5L Malnutrition Nutritional status Postoperative complications Enhanced recovery

Interventions

Participants receive preoperative nutritional counseling delivered via a standardized video at the time of surgical scheduling. The video provides information equivalent to standard counseling, inclu
Experimental Behavioral,No Intervention Other
Video-assisted nutritional counseling,Standard preoperative counseling

Sponsors

Department of Obstetrics and Gynecology, Phramongkutkao Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Female patients aged 20 to 70 years undergoing planned elective gynecologic surgery Able to 2.understand study procedures and communicate in Thai 3.Able to receive oral nutritional intake 4.Provide written informed consent prior to participation

Exclusion criteria

Exclusion criteria: 1.Unable to understand or communicate in Thai 2.Unable to receive oral nutrition 3.Diagnosed malnutrition or high nutritional risk at baseline 4.Active infection at the time of enrollment 5.Pregnant or breastfeeding women 6.Sensory or cognitive impairment that limits understanding of the intervention such as severe 7.visual impairment hearing impairment or cognitive dysfunction 8.Refusal or inability to provide informed consent

Design outcomes

Primary

MeasureTime frame
Change in quality of life Baseline (at enrollment), preoperative admission day, and postoperative day 3 (at discharge) EuroQol-5 Dimension 5 Level (EQ-5D-5L) score

Secondary

MeasureTime frame
Postoperative complications Up to 30 days postoperatively Proportion of participants with at least one postoperative complication within 30 days assessed from medical records,Change in nutritional status Baseline to postoperative day 3 Change in nutritional status assessed by Nutrition Risk Score NRS 2002 and Nutrition Alert Form NAF from baseline to postoperative day 3,Patient satisfaction Postoperative day 3 Patient satisfaction score assessed by Likert scale questionnaire at postoperative day 3

Countries

Thailand

Contacts

Public ContactPrimnara Techasontichai

Department of Obstetrics and Gynecology, Phramongkutklao Hospital

primnara.tec@pcm.ac.th0881971119

Outcome results

None listed

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