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Impact of Interactive Video Health Intervention on Quality of Life After Bowel Obstruction Surgery

C

Changsha Fourth Hospital

Status

Completed

Conditions

Postoperative Complications
Intestinal Obstruction

Treatments

Behavioral: Conventional care
Behavioral: Interactive Video Health Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT07258017
CSSDSYY-YXLL-SC-2024-02-20

Details and patient eligibility

About

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).

Enrollment

462 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with early postoperative intestinal obstruction after abdominal surgery based on clinical symptoms, physical examination and imaging
  • Aged between 18 and 75 years
  • With basic cognitive ability and comprehension
  • Informed consent obtained directly from patients; family members provided supplementary consent

Exclusion criteria

  • Serious underlying diseases
  • Serious mental diseases
  • Audio-visual impairment that prevents normal reception of interactive video information
  • Poor compliance

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

462 participants in 2 patient groups

Conventional Care Control Group
Active Comparator group
Treatment:
Behavioral: Conventional care
Interactive Video Health Intervention Group
Experimental group
Treatment:
Behavioral: Interactive Video Health Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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