Association Between Work-Related Stress and Peripheral Neuropathic Pain in Female Breast Cancer Post CT

NCT07055711 | Active Not Recruiting DMC

• 1 other identifier: DPT/Batch-Fall20/1016
• Study Type: observational
• Target: 45
• Locations: 1 country
• Sites: 1

Brief Summary

This research aims to find the association between work-related stress and peripheral neuropathic pain in female breast cancer survivors post-chemotherapy.

Conditions

Peripheral Neuropathy

Outcome Measures

Primary Outcomes (2)

• Douleur Neuropathique 4 (DN4) Questionnaire

  The DN4 questionnaire is used to assess the neuropathic pain, if the score is \> 4 it indicates the neuropathic pain is present while \<3 than is unlikely.

  6 Month

• visual analog scale

  The visual analog scale provide quantitative measurement of pain level which is from no pain to severe pain . The range of the scale is in between 0-10mm. 0-4 is consider as no pain, 5-44 is consider as mild pain,45-74 is moderate and \> 75 is consider as severe pain.

  6 Months

Interventions

Peripheral Neuropathic Pain DIAGNOSTIC_TEST

to find out the association between work-related stress and peripheral neuropathic pain in female breast cancer survivors post-chemotherapy.

Eligibility Criteria

• Age: 21 Years - 51 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

to find out the Association Between Work-Related Stress and Peripheral Neuropathic Pain in Female Breast Cancer

You may qualify if:

• Females who have completed chemotherapy at least o1 year prior to study.
• Aged 29-51.
• Females who is currently employed.
• Females who have done chemotherapy for stage 1,2,3.
• Females who underwent chemotherapy cycles 6-8.
• Females who are willing to participate in the study

You may not qualify if:

• Females suffering from psychiatric conditions such as anxiety and depression.
• Females suffering from diabetes.
• Females who have active cancer.
• Females with mastectomy.
• Absent from treatment for more than 2 weeks will be excluded from the study.

Sponsors & Collaborators

• Superior University: lead

Study Sites (1)

Lahore City

Lahore, Pakistan

Location

MeSH Terms

Conditions

Peripheral Nervous System Diseases

Condition Hierarchy (Ancestors)

Neuromuscular Diseases; Nervous System Diseases

Study Design

• Study Type: observational
• Observational Model: CASE CONTROL
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: June 28, 2025
• First Posted: July 9, 2025
• Study Start: March 3, 2025
• Primary Completion: June 1, 2025
• Study Completion: September 1, 2025
• Last Updated: July 9, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will not share

Locations

PA (1)