- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07570004
The Effect of Preoperative Abdominal Massage on Postoperative Constipation
The Effect of Preoperative Abdominal Massage on The Development of Postoperative Constipation: A Randomised Controlled Study
The aim of this clinical study is to determine whether preoperative abdominal massage has an effect on the development of postoperative constipation. The main questions it aims to answer are:
• Does preoperative abdominal massage improve postoperative stool consistency? • Does preoperative abdominal massage prevent constipation? To see if abdominal massage is effective in preventing constipation, researchers will not apply any treatment to the second group and will compare the two groups.
Participants will:
- Provide researchers with information about their preoperative and postoperative stool consistency and constipation status.
- Inform the researchers if the group that received the massage experiences any adverse effects from the massage.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Abdominal massage, being a low-cost, non-invasive procedure with no known harmful side effects, and one that nurses can integrate into clinical practice, plays an important role in the management of constipation.
This study is a single-center, randomized controlled experimental trial planned to be conducted in the General Surgery Department of a Training and Research Hospital in Istanbul. Standard operating procedures for patient recruitment, data collection, data management, adverse event reporting, and change management processes have been predefined. The experimental group will receive abdominal massage twice daily for 15 minutes, while the control group will continue with routine care. Adverse events will be recorded after each session, and necessary protocol changes will be documented in accordance with formal change management procedures. The sample size was determined based on a power analysis performed with G*Power 3.1; 30 participants were planned for each group (total n=60; α=0.05, power=0.80). A complete case analysis approach will be adopted for missing data resulting from data inconsistencies, out-of-range results, or unanswered items, and group assignments will continue until data is complete. In accordance with the statistical analysis plan, the Mann-Whitney U test will be used for between-group comparisons and the Wilcoxon test for within-group comparisons for the Bristol Stool Scale (BSS) score, which is the primary outcome measure; For the secondary outcome measure, stool type distribution, the Chi-square test will be applied. Effect size will be reported using Cohen's d and odds ratio, and the statistical significance threshold will be set at p<0.05.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Istanbul
-
Istanbul, Istanbul, Tyrkiet (Türkiye)
- Health Sciences University Sultan Abdülhamid Han Training and Research Hospital
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion criteria:
- Being hospitalized in the General Surgery Department
- Experiencing constipation
- Being 18 years of age or older
- Having the cognitive ability to answer questions
- Voluntary participation in the study
Exclusion criteria:
- Being under 18 years of age
- Not experiencing constipation
- Having a condition that contraindicates abdominal massage (active intra-abdominal pathology, open wound, thrombocytopenia, etc.)
- Insufficient cognitive ability
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Ingen indgriben: Kontrolgruppe
|
|
|
Eksperimentel: Abdominal Massage İnterventional Group
Massage Group
|
The procedure will be followed using a protocol prepared by researchers based on a literature review.
Massage sessions are scheduled for 10:00 AM and 4:00 PM, 30 minutes after a meal.
The massage duration is 15 minutes.
The frequency of massage is twice a day.
Necessary tools and equipment include liquid petroleum jelly and a towel.
The massage techniques include effleurage (superficial and deep), petrissage, and vibration.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
BSS score
Tidsramme: BSS score preoperative period and postoperative 24. hour
|
According to the Bristol Stool Scale, a score of 1-2 indicates "hard stools," 3-4-5 indicates "normal stools," and 6-7 indicates "soft-watery stools (diarrhea)."
|
BSS score preoperative period and postoperative 24. hour
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Stool type distribution/constipation
Tidsramme: preoperative period and postoperative 24. hour
|
Stool type: hard/normal
|
preoperative period and postoperative 24. hour
|
Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
Generelle publikationer
- McClurg D, Lowe-Strong A. Does abdominal massage relieve constipation? Nurs Times. 2011 Mar 29-Apr 4;107(12):20-2.
- Celik S, Atar NY, Ozturk N, Mendes G, Kuytak F, Bakar E, Dalgiran D, Ergin S. Constipation risk in patients undergoing abdominal surgery. Iran Red Crescent Med J. 2015;17(6):e23632. doi: 10.5812/ircmj.23632
- 1. Olgun S, Eser I. The effect of abdominal massage on chronic constipation and constipation quality of life in elderly: a randomized controlled trial. Int J Med Res Health Sci. 2021;10(6):20-30.
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 24/11/2022-984
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Abdominal Massage
-
Ain Shams UniversityAfsluttet
-
Hospital de GranollersAfsluttetAkut divertikulitisSpanien
-
Buddhist Tzu Chi General HospitalAfsluttetIrritabelt tarmsyndrom | Funktionelle gastrointestinale lidelser | Sunde emner | Laryngopharyngeal refluksTaiwan
-
University of PotsdamIkke rekrutterer endnuDysmenoré | Dysmenoré Primær | Dysmenoré Sekundær | Dysmenoré Symptom
-
Princess Anna Mazowiecka Hospital, Warsaw, PolandJagiellonian University; Ujastek Obstetrics and Gynaecology Hospital; University...UkendtNekrotiserende enterocolitisPolen
-
South Valley UniversityAfsluttetProlaps GenitalEgypten
-
Turku University HospitalAfsluttet
-
Mayo ClinicAfsluttetOrtostatisk hypotension | Autonomisk fiaskoForenede Stater
-
Sheba Medical CenterAfsluttetReparation af kejsersnitIsrael
-
St George's Healthcare NHS TrustAfsluttetHysterektomiDet Forenede Kongerige