NCT07667985

Brief Summary

As people grow older, it is common to experience a drop in physical stamina and memory functions. This can make recovering from daily physical and mental fatigue more difficult, which directly impacts an individual's independent daily life and overall quality of life. "Cognitive reserve" is a term that describes the brain's built-in resilience. Built over a lifetime through education, work, and social activities, a higher cognitive reserve acts like a buffer, helping the brain adapt to stress and aging. While research shows that a high cognitive reserve protects against conditions like dementia, we still do not fully understand how it helps older adults bounce back from normal, everyday physical and mental exhaustion. The goal of this study is to investigate how cognitive reserve levels influence how individuals aged 65 and older perceive their recovery after experiencing physical and mental fatigue. What the Study Involves The researchers will evaluate participants aged 65 and older to measure their baseline cognitive reserve levels. The study will look closely at how these levels affect the participants': Ability to cope with daily physical and mental fatigue. Need for rest and rest patterns. Time and ability to return to normal daily activities. Overall perception of their mental and physical recovery. Expected Outcome By understanding this relationship, the study aims to fill a gap in medical literature and help healthcare providers design better, more personalized rehabilitation and lifestyle support programs to improve the quality of life for older adults.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
2mo left

Started Jun 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress47%
Jun 2026Sep 2026

First Submitted

Initial submission to the registry

June 19, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

June 20, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 25, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 21, 2026

Expected
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 22, 2026

Last Updated

June 25, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

June 19, 2026

Last Update Submit

June 19, 2026

Conditions

Keywords

agingcognitive reservefatiguePost-Fatigue Recovery

Outcome Measures

Primary Outcomes (1)

  • Cognitive Reserve Level

    Cognitive Reserve Index questionnaire (CRIq):It assesses an individual's cognitive reserve by compiling information about that individual's entire adult life. The assessment will be conducted with the aid of a guide containing guidelines.

    Baseline

Secondary Outcomes (1)

  • Perception of Coping and Recovery After Mental and Physical Fatigue

    Baseline

Eligibility Criteria

Age65 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of community-dwelling older adults aged 65 and over.The sample will include individuals who are independently mobile, able to perform activities of daily living, and free of severe cognitive impairments or acute medical conditions that would prevent them from understanding the research protocol or reporting their perception of fatigue and recovery.

You may qualify if:

  • being 65 years of age or older,
  • not having any neurological, psychiatric, or systemic disease that would affect one's mental state, and not using any medication for these conditions.

You may not qualify if:

  • Being younger than 65 years old,
  • having an illness or taking medication that affects mental health, or being
  • unable to complete the questionnaires.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Uşak University

Uşak, Uşak, 64000, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Mental FatigueFatigue

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehavior

Study Officials

  • Elif Tuncay, PhD

    Uşak University

    PRINCIPAL INVESTIGATOR
  • Kevser GÜRSAN, PhD

    Uşak University

    STUDY DIRECTOR
  • Emre Cengiz, PhD

    Uşak University

    STUDY CHAIR
  • Elif Gür Kabul, PhD

    Uşak University

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

June 19, 2026

First Posted

June 25, 2026

Study Start

June 20, 2026

Primary Completion (Estimated)

September 21, 2026

Study Completion (Estimated)

September 22, 2026

Last Updated

June 25, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations