Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Constipation Prevention Checklist in hip surgery patients

Official title: The Effect of Monitoring Constipation Prevention Practices in Hip Surgery Patients With the Perioperative Constipation Prevention Checklist on Patient Outcomes: A Randomized Controlled Study

Run by Cumhuriyet University · NCT07895316 · Data updated 2026-11-12

A simple checklist is used to see if hip surgery patients can stay regular by staying hydrated, eating well, moving early, and using abdominal massage.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment124 (estimated)
SponsorCumhuriyet University
Academic / other
Locations1 site (Sivas)
StatusRecruiting
StartedOctober 12, 2026
Main results expectedJuly 2027
Study endsDecember 2027
Registry record updatedOctober 26, 2026
Trial IDNCT07895316 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 18 or older undergoing primary hip surgery for fracture, able to communicate in Turkish, and able to participate for at least 3 days postoperatively.

Probably not a fit

Patients with chronic constipation, certain GI conditions, prior GI surgeries, or contraindications to mobilization or abdominal massage may not benefit from this checklist.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional trial tests whether a standardized perioperative constipation prevention checklist improves bowel function and recovery after hip surgery. Participants are adults undergoing primary hip surgery due to fracture and monitored for at least 3 days postoperatively. The checklist guides risk assessment and tracks fluids, nutrition, mobilization, and abdominal massage to see if these practices reduce constipation severity and improve recovery quality. The study will compare outcomes related to bowel sounds, constipation severity, and overall recovery between those using the checklist and usual care. The lead sponsor is Cumhuriyet University in Sivas, Turkey.

Why it matters

Potential benefit: If successful, the checklist could help reduce postoperative constipation and enhance recovery after hip surgery.

How similar studies have gone: There is limited evidence on standardized perioperative constipation checklists; prior data on similar approaches are not definitive.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients who will undergo primary hip surgery due to a fracture,
* 18 years of age and older,
* Able to communicate in Turkish and possess the cognitive/communicative competence to respond to data collection tools,
* Without hearing problems that would impede communication (including those using hearing aids),
* Expected to be monitored for at least 3 days postoperatively,
* Patients who volunteer to participate in the study and provide written informed consent.

Exclusion Criteria:

* Patients with diagnosed chronic constipation, irritable bowel syndrome, or inflammatory bowel disease,
* Patients with a history of gastrointestinal surgery or a stoma,
* Patients with acute abdomen, suspected bowel obstruction, gastrointestinal perforation, active gastrointestinal bleeding, etc.,
* Patients with abdominal wall or abdominal clinical conditions that prevent abdominal massage,
* Patients with contraindications for mobilization and who have an external fixator,
* Patients with (Mini Cognitif Test) Mini-Cog \<3,
* Patients with active psychiatric illness that would prevent participation in the study or data collection process,
* Patients with American Society of Anesthesiologists IV or V (ASA IV or V),
* Patients whose surgery has been postponed,
* Patients who have undergone secondary hip surgery.

Where it's running

  • Sivas Cumhuriyet University
    Sivas, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 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.