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Clinical Trials/NCT01478295
NCT01478295
Completed
Not Applicable

Effectiveness of Nursing Intervention on Quality of Life of Older Caregivers: Clinical Trial Randomised by Clusters

Gerencia de Atención Primaria, Madrid1 site in 1 country266 target enrollmentJune 2013
ConditionsQuality of Life

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Quality of Life
Sponsor
Gerencia de Atención Primaria, Madrid
Enrollment
266
Locations
1
Primary Endpoint
Perceived quality of life
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effectiveness of a structured nursing intervention (PCE), including two types of intervention defined in the literature (coping strategies promoting social support and empowerment through health education), which has an effect on the perceived quality of life for the caregiver, when compared with conventional intervention or non-support.

Detailed Description

Aim: to compare the effectiveness of a standardized care plan (SCP) compared to the usual nursing intervention to improve the quality of life for primary caregivers over 65 years old measured through points change with the EuroQol-5D (EQ-5D) scale. Secondary objectives: Evaluate the influence of prognostic variables on quality of life of caregiver. Describe the level of caregiver burden. Describe the socio-demographic profile of the dependent person and caregiver. Method: Design: cluster randomized trial. Setting: study in Health Centers Primary Care of Area of Madrid Health Service. Subjects: unit of randomization: primary healthcare centres. Analysis unit: caregivers over 65 years old. Intervention: The SCP in the treatment group and the usual intervention in the control group. Sample size adjusted for design effect= 218 (109 in each arm). Main response variable: perceived quality of life (EQ-5D). Secondary response variables: nursing diagnosis, Zarit Caregiver Burden Interview, objective overload level. Prognostic variables:Dependent person-related: dependence level (Barthel, Lawton-Brody), cognitive dysfunction (Pfeiffer). Caregiver-related: depression scale (Yesavage), anxiety level (Goldberg), family function (family Apgar). Sociodemographic variables. Data Analysis: Analysis of main effectiveness by intention to treat, comparing the difference in units on the EQ-5D scale before and post- intervention in both groups at 0, 6, 12 and 18 months. The estimation adjusted, using logistic regression with aleatory effects, those data that can act as confounding factors or change the effect.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
December 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Gerencia de Atención Primaria, Madrid
Responsible Party
Principal Investigator
Principal Investigator

Milagros Rico Blazquez

Nurse

Gerencia de Atención Primaria, Madrid

Eligibility Criteria

Inclusion Criteria

  • Not psychological treatment or social support during the study period.
  • Be able to follow the trial's demands.
  • Experience of caring for at least 6 months in a year.
  • Caregivers who consent to take part.

Exclusion Criteria

  • Caregivers of patients hospitalized during the initial data collection.
  • Caregivers of institutionalized patients.
  • Severe psychiatric conditions including depression and major affective pictures.
  • Paid caregivers.
  • Experience as a caregiver for less than a month.

Outcomes

Primary Outcomes

Perceived quality of life

Time Frame: Change from baseline in quality of life at 18 months after the intervention

Perceived quality of life: Quality of life measured by EuroQol (EQ5D) Scale Change from baseline in quality of life at 18 months after the intervention

Secondary Outcomes

  • Nursing diagnosis(Change from Baseline in Nursing diagnosis at 18 months after the intervention)
  • Caregiver Burden(Change from Baseline in Caregiver Burden at 18 months after the intervention)
  • Depression scale(Change from Baseline in Depression scale at 18 months after the intervention)
  • Family function(Change from Baseline in Family function at 18 months after the intervention)
  • Anxiety level(Change from Baseline in Anxiety level at 18 months after the intervention)

Study Sites (1)

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