NCT07373860

Brief Summary

The primary aim of this study is to investigate the relationship between frailty status and pain type, pain localization, and the Geriatric Nutritional Risk Index (GNRI) in individuals aged 65 years and older who present to an pain clinic with chronic pain. The secondary aim is to evaluate the level of interaction among these parameters and to contribute to a holistic approach to pain management in older adults.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
393

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2026

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

January 15, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 28, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 12, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 12, 2026

Completed
Last Updated

May 13, 2026

Status Verified

May 1, 2026

Enrollment Period

4 months

First QC Date

January 15, 2026

Last Update Submit

May 12, 2026

Conditions

Keywords

chronical painneuropathic painNociceptive Pain

Outcome Measures

Primary Outcomes (1)

  • primary outcome

    Frailty status determined according to the Fried Frailty Criteria (Frailty Phenotype). Frailty will be classified as robust (0 criteria), pre-frail (1-2 criteria), or frail (≥3 criteria) based on the presence of unintentional weight loss, exhaustion, low physical activity, slowness, and weakness.

    baseline

Secondary Outcomes (6)

  • Secondary outcome

    baseline

  • Secondary Outcome Measure

    baseline

  • Secondary outcome meaaure

    Baseline

  • Secondary outcome

    Baseline

  • Secondary outcome

    During the 3-month follow-up period.

  • +1 more secondary outcomes

Study Arms (1)

Elderly Chronic Pain Cohort

The Elderly Chronic Pain Cohort consisted of individuals aged 65 years and older who presented to the pain outpatient clinic with complaints of chronic pain and met the study inclusion criteria. All eligible participants were consecutively enrolled during the study period. Frailty status, nutritional risk, and pain-related characteristics were systematically assessed at baseline. Subgroup analyses were performed according to frailty statu

Eligibility Criteria

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

Patients who have chronical pain for more than months and older than 65 years old

You may qualify if:

  • Age 65 years or older Diagnosis of chronic pain (duration \> 3 months)

You may not qualify if:

  • Acute pain complaint Pain related to malignancy Severe communication impairment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Bilkent City Hospital

Ankara, Cankaya, Turkey (Türkiye)

Location

Related Publications (1)

  • Saito T, Liu X, Yatsugi H, Chu T, Yokote T, Kishimoto H. Relationship Between Chronic Pain Types (Nociceptive and Neuropathic-Like Symptoms) and Frailty in Community-Dwelling Japanese Older Adults: A Cross-Sectional Study. J Pain Res. 2023 Aug 1;16:2675-2684. doi: 10.2147/JPR.S402002. eCollection 2023.

MeSH Terms

Conditions

NeuralgiaNociceptive Pain

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assoc. prof.

Study Record Dates

First Submitted

January 15, 2026

First Posted

January 28, 2026

Study Start

January 1, 2026

Primary Completion

May 12, 2026

Study Completion

May 12, 2026

Last Updated

May 13, 2026

Record last verified: 2026-05

Locations