Viewing Study NCT06390254



Ignite Creation Date: 2024-05-06 @ 8:28 PM
Last Modification Date: 2024-10-26 @ 3:28 PM
Study NCT ID: NCT06390254
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-30
First Post: 2024-04-21

Brief Title: Resilience-Building Nursing Intervention for Elderly Well-being
Sponsor: Cairo University
Organization: Cairo University

Study Overview

Official Title: Effectiveness of a Resilience-Building Nursing Intervention on Psychological Well-being in Community-Dwelling Older Adults
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The objective of this study is to evaluate the impact of a resilience-enhancing nursing intervention on the psychological well-being of older adults living in the community Participants will benefit from individualized nursing support designed to bolster their resilience and coping skills This intervention will be customized to meet personal requirements and provided in a nurturing setting Engaging in this study could result in enhanced well-being and life quality Although some minor discomforts may arise during assessments or interventions the confidentiality and rights of the participants will be rigorously safeguarded
Detailed Description: Background

As the global population ages there is an increasing need to address the psychological well-being of older adults living independently in the community Previous research has highlighted the importance of resilience in maintaining mental health and coping with life stressors among older individuals However there is limited evidence on the effectiveness of specific interventions aimed at enhancing resilience in this population

Objective

The primary objective of this study is to evaluate the effectiveness of a resilience-building nursing intervention in improving the psychological well-being of community-dwelling older adults Secondary objectives include assessing the impact of the intervention on factors such as social support coping strategies and quality of life

Study Design

This study will employ a randomized controlled trial design Participants will be randomly assigned to either the intervention group receiving the resilience-building nursing intervention or the control group receiving standard care

Intervention

The resilience-building nursing intervention will consist of individualized sessions delivered by trained nurses The intervention will focus on enhancing participants39 resilience through skill-building exercises cognitive-behavioral techniques and psychoeducation Sessions will be tailored to address the unique needs and challenges of each participant

Participants

The target population for this study includes community-dwelling older adults aged 65 and above who are experiencing mild to moderate psychological distress Participants will be recruited from community centers senior living facilities and primary care clinics

Procedures

Participants will undergo baseline assessments to collect demographic information and baseline measures of psychological well-being Those assigned to the intervention group will receive the resilience-building nursing intervention over a specified period with follow-up assessments conducted at regular intervals to evaluate outcomes

Outcome Measures

Primary outcome measures will include changes in psychological well-being as assessed by standardized scales such as the Geriatric Depression Scale and the Psychological Well-being Scale Secondary outcome measures will include social support coping strategies and quality of life

Statistical Analysis

Data will be analyzed using appropriate statistical methods including t-tests chi-square tests and linear regression Sample size calculations will ensure adequate power to detect meaningful differences between groups

Ethical Considerations

This study will adhere to ethical principles outlined in the Declaration of Helsinki Informed consent will be obtained from all participants and measures will be taken to ensure participant confidentiality and privacy

Data Management

Data will be collected using secure electronic data capture systems and stored in accordance with institutional guidelines and data protection regulations

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None