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Nursing Homes on Constipation and General Comfort

G

Giresun Huzurevi Yaşlı Bakım ve Rehabilitasyon Merkezi

Status

Completed

Conditions

Constipation
Nursing Caries

Treatments

Other: reminiscence therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06788392
AIBU-SBF-KK-01
Kevser KASAP (Other Identifier)

Details and patient eligibility

About

The Effect of Reminiscence Therapy on Constipation Applied to Elderly Individuals Staying in a Nursing Home in Giresun Province

Full description

Research; This study will be conducted to determine the effect of reminiscence therapy, given once or twice a week to elderly people living in nursing homes, on constipation by reducing stress levels. It is thought that the results obtained will provide evidence for reducing constipation, which significantly limits life. Patients who complain of constipation at the Nursing Home Elderly Care and Rehabilitation Center, who voluntarily agree to participate in the research and who meet the sample selection criteria will be included in the study. Patient information will be collected and the research pre-test, post-test and application will be carried out face to face.

Enrollment

70 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria for the study:

  • Those aged 65 and over,
  • Able to answer all questions and be communicative,
  • Scoring 24 or above from the Mini Mental test,
  • Agreeing to participate in the research,
  • Diagnosed with constipation by the institution physician and meeting the Rome III Constipation Diagnostic Criteria,
  • There is no deterioration in skin integrity or infection in the abdominal area,
  • No diarrhea,
  • Individuals without a history of abdominal surgery will be included in the study.

Exclusion Criteria

  • Psychiatric drug users,
  • Those who score below 24 on the Mini Mental Test,
  • Those who do not meet the Rome III Diagnostic Criteria for Constipation,
  • Those with impaired skin integrity or infection in the abdominal area,
  • People with diarrhoea,
  • History of abdominal surgery Those who refused to participate in the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

interventional
Experimental group
Description:
Group receiving reminiscence therapy 2 days a week
Treatment:
Other: reminiscence therapy
control
No Intervention group
Description:
The group in which no intervention and receiving routine nursing care

Trial contacts and locations

1

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Central trial contact

SERPİL HEMŞİRE; KEVSER K HEMŞİRE

Data sourced from clinicaltrials.gov

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