Physiotherapy after emergency laparotomy for older adults

Effect of Postoperative Physiotherapy on Postoperative Outcomes of Elderly Patients Undergoing Emergency Laparotomy

Not applicable Interventional University of Cyprus · NCT07504185

This study will test whether a five-day structured physiotherapy program after emergency open abdominal surgery helps people aged 65 and older recover function faster and have fewer complications.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment250 (estimated)
Ages65 Years and up
SexAll
SponsorUniversity of Cyprus Academic / other
Locations1 site (Nicosia)
Trial IDNCT07504185 on ClinicalTrials.gov

What this trial studies

This is a multicenter, randomized, parallel-group trial enrolling patients aged 65 and older who undergo emergency laparotomy and are clinically stable on the surgical ward. Participants are randomized 1:1 to a standardized, progressive five-day postoperative physiotherapy package (early supervised mobilization, coached breathing and airway clearance exercises, and supported self-practice with family/caregiver engagement) or to usual postoperative care. Functional recovery is measured with validated tools during the hospital stay and at 30- and 90-day follow-up, with secondary outcomes including postoperative and pulmonary complications, length of stay, mortality, and health-related quality of life. Analyses follow the intention-to-treat principle and use computer-generated allocation after surgery.

Who should consider this trial

Good fit: Ideal candidates are patients aged 65 or older undergoing emergency laparotomy who can stand briefly with minimal assistance and can provide informed consent or have a legal representative do so.

Not a fit: Patients with significant cognitive impairment (AMTS < 6), severe pre-existing mobility disabilities, contraindications to physiotherapy, palliative/end-of-life procedures, transfers from other hospitals, or negative laparotomies are excluded and unlikely to benefit.

Why it matters

Potential benefit: If successful, the program could speed functional recovery, reduce pulmonary and other postoperative complications, and shorten hospital stays for older patients after emergency laparotomy.

How similar studies have performed: Early mobilization and physiotherapy programs have shown benefits in elective and general surgical populations, but randomized evidence specifically in older emergency laparotomy patients is limited.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients aged ≥ 65 years
* Undergoing emergency laparotomy with or without stoma creation (adhesiolysis, right hemicolectomy, total colectomy, Hartmann's procedure, cholecystectomy, abscess drainage).

Able to provide informed consent or have a legally authorized representative provide consent.

Able to maintain an upright standing position for at least one minute with minimal or no assistance.

Exclusion Criteria:

* Patients with Dementia (Abbreviated Mental Test Score \< 6)
* Pre-existing severe disabilities affecting mobility
* Patients with contraindications to physiotherapy (e.g., severe cardiopulmonary instability)
* Patients transferred postoperatively from other hospitals
* Patients who underwent no intervention during laparotomy (negative laparotomies)
* Patients undergoing palliative procedures and at the end of life

Where this trial is running

Nicosia

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Emergency Abdominal Surgerypostoperative recovery, elderly, emergency abdominal surgeryPhysiotherapy intervention
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.