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Not yet recruiting NCT07437014

The Effect of Abdomınal Massage and Warm Water Consumptıon on Postoperatıve Constıpatıon Development and Qualıty of Recovery in Patıents Undergoıng Hıp Fractures Surgery

No phase Interventional Hip Fracture Surgeries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ABDOMINAL MASSAGE AND WARM WATER CONSUMPTION, abdominal massage, Control (Standard treatment).
Who it may be relevant to
Registry conditions: Hip Fracture Surgeries. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Effect of Abdomınal Massage and Warm Water Consumptıon on Postoperatıve Constıpatıon Development and Qualıty of Recovery in Patıents Undergoıng Hıp Fractures Surgery: A Randomızed Comparatıve Study

Overview

There is a need for studies investigating the effects of abdominal massage and warm water consumption on the development of postoperative constipation and quality of recovery in patients who have undergone hip fracture surgery. The aim of the study is to investigate the effects of abdominal massage and warm water consumption on the development of postoperative constipation quality of recovery in patients who have undergone hip fracture surgery. The study will be conducted as a prospective, parallel, three-group (1:1:1) randomized controlled trial to determine the effect of abdominal massage alone versus standard care in preventing the development of postoperative constipation in patients who underwent surgery for hip fracture. The following instruments will be used to collect study data: "Patient Demographic Information Form", "Constipation Risk Assessment Scale" for determining the constipation risk group and for randomization, "Bristol Stool Scale" for determining the type of constipation, "Constipation Assessment Scale" for determining the severity of constipation, and "Quality of Recovery-40 Questionnaire". For data analysis, parametric (Independent Samples T-Test, ANOVA) or non-parametric tests (Mann-Whitney U, Kruskal-Wallis H) will be used for pairwise and multiple group comparisons, depending on the distribution of the data. The Chi-Square test will be used for categorical data, and logistic regression analysis will be performed to determine the effect of continuous variables obtained from constipation development status and patient follow-up on the development or absence of constipation.

Interventions

  • Behavioral ABDOMINAL MASSAGE AND WARM WATER CONSUMPTION
    The effect of abdominal massage and warm water consumptione on postoperative constipation.
  • Other abdominal massage
    abdominal massage on postoperative constipation.
  • Other Control (Standard treatment)
    standart protocol on the development of postoperative constipation

Primary outcome measures

  • constipation risk assessment [Time frame: baseline (day 0)]
  • Occurrence of postoperative constipation [Time frame: Postoperative Days 1-15]
  • Postoperative Constipation Severity [Time frame: postoperative daily from Day 1 to Day 15"]
  • classify faeces [Time frame: Postoperative Days 1-15]
Secondary outcome measures (1)
  • quality of recovery [Time frame: postoperative day 15]

Eligibility criteria

Inclusion criteria

  • Being 18 years of age or older
  • Agreeing to participate in the study
  • Undergoing open surgical treatment due to a hip fracture classified as 31A, 31B, or 31C according to the AO/OTA classification
  • Initiation of postoperative oral feeding

Exclusion criteria

  • Communication problems (speech and hearing impairments)
  • Neurological and psychiatric problems such as Alzheimer's or dementia
  • Problems preventing abdominal massage (surgery, wound site)
  • Regular laxative use before surgery
  • Previous colon surgery - physiological and structural abnormalities in the anal region that may hinder bowel movements
  • Use of medications that reduce bowel motility before surgery (antipsychotics, antidepressants, etc.)
  • Diagnosis of chronic constipation made by a physician before surgery
  • Difficulty transitioning to oral feeding and inability to eat orally
  • Multiple traumas affecting mobilization in addition to a hip fracture
  • Surgery for hip fracture performed using a minimally invasive method

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07437014 · E2-26-14078

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗