Last reviewed · How we verify
NCT07258017
Impact of Interactive Video Health Intervention on Quality of Life After Bowel Obstruction Surgery
NA trial testing Conventional care in Intestinal Obstruction in 462 participants. Completed in 24 January 2025.
13 January 2025
Quick facts
| Lead sponsor | Changsha Fourth Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 462 |
| Start date | 10 January 2019 |
| Primary completion | 13 January 2025 |
| Estimated completion | 24 January 2025 |
| Sites | 1 location across China |
Drugs / interventions tested
- Conventional care
- Interactive Video Health Intervention
Conditions studied
- Intestinal Obstruction — all drugs for Intestinal Obstruction →
- Postoperative Complications — all drugs for Postoperative Complications →
Sponsor
Changsha Fourth Hospital
Who can join
Adults 18 to 75, any sex, with Intestinal Obstruction or Postoperative Complications. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Objective: To investigate the multidimensional effects of an interactive video health intervention on the quality of life and clinical rehabilitation indicators of patients with early postoperative bowel obstruction. Methods: The study consists of two phases. Phase 1 (January 2019-December 2020) involves the development and psychometric validation of a Postoperative Quality of Life Assessment Scale for Early Intestinal Obstruction, with approximately 150 patients. Phase 2 (January 2021-January 2025) is a randomized controlled trial enrolling about 310 eligible patients (aged 18-75 years, with basic cognitive ability, diagnosed with early postoperative bowel obstruction after abdominal surgery). Participants are randomly assigned to either a control group (conventional care, including condition monitoring, basic treatment, and non-structured health education) or a study group (conventional care plus an interactive video health intervention consisting of five modular videos covering disease knowledge, rehabilitation, and diet, initiated 24 hours post-surgery). Primary and secondary outcomes will include quality of life (assessed with the validated scale), clinical rehabilitation indicators (such as obstruction relief time and hospitalization duration), electrogastrogram parameters, and gut microbiota diversity (16S rRNA sequencing).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Multidimensional impact analysis of interactive video health intervention on quality of life and clinical rehabilitation indicators in patients with early postoperative bowel obstruction: a randomized controlled trial.
Yao L, Wu D, Liu J, Zhang X, et al · · 2026 · PMID 41507597 · DOI 10.1007/s00384-025-05051-0
Verify or expand the search:
- PubMed search for NCT07258017
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Conventional care
Trials testing the same drug.
- NCT07395648 — Foundation Model for Post-MI Cardiovascular Event Alert Using Huawei Watch · NA · not yet recruiting
- NCT07248813 — Telerehabilitation Program to Improve Function in People With Chronic Low Back Pain Compared With Conventional Care · NA · recruiting
- NCT06672081 — Early Catheter-directed Treatment of High Risk Pulmonary Embolism · NA · recruiting
- NCT06293170 — Automated Screening for Clinically Ascertained Loss of Cerebral Functions · NA · not yet recruiting
- NCT06309875 — Effect of the PLAN CUIDARTE on the Caregiving Competence of People With Heart Failure · Phase 2 · unknown
Other recruiting trials for Intestinal Obstruction
Currently open trials in the same condition.
- NCT07432542 — Pelvic Floor Peritoneal Closure to Prevent Postoperative Ileus in Mid-Low Rectal Cancer Surgery · NA · active not recruiting
- NCT06245577 — Biological Mesh Versus Synthetic Mesh in Interdisciplinary RRP With SCP · NA · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07258017 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Changsha Fourth Hospital
- Last refreshed: 2 December 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07258017.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing