NCT06873529

Brief Summary

The aim of this study was to investigate the experiences of women with spinal cord injury regarding fertility, contraception and pregnancy.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
70

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2025

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

First Submitted

Initial submission to the registry

March 7, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 12, 2025

Completed
8 days until next milestone

Study Start

First participant enrolled

March 20, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 2, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 2, 2026

Completed
Last Updated

March 27, 2026

Status Verified

March 1, 2026

Enrollment Period

12 months

First QC Date

March 7, 2025

Last Update Submit

March 26, 2026

Conditions

Spinal Cord Injury

Keywords

fertilitycontraceptionpregnancy

Outcome Measures

Primary Outcomes (1)

  • Evaluation of experiences with fertility, contraception and pregnancy

    The content of the survey used in the study was created by the research team after reviewing the current literature examining the parameters related to fertility, contraception and pregnancy in women with spinal cord injury. The survey consists closed-ended (e.g., use of a five-point Likert scale to assess whether spinal cord injury affects the decision to have children (Higher scores mean worse outcome)) and open-ended questions (e.g., What is the reason for choosing the contraceptive method used?)

    through study completion, an average of one month

Study Arms (1)

spinal cord injury group

The evaluation of experiences of women with spinal cord injury regarding fertility, contraception and pregnancy

Eligibility Criteria

Age18 Years - 55 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Women with spinal cord injury who have been injured for at least 1 year

You may qualify if:

  • Ages 18-55
  • Post-spinal cord injury period \> 1 year

You may not qualify if:

  • Having cognitive impairment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Spinal Cord Injuries

Condition Hierarchy (Ancestors)

Spinal Cord DiseasesCentral Nervous System DiseasesNervous System DiseasesTrauma, Nervous SystemWounds and Injuries

Study Officials

  • Merve Örücü Atar

    Ankara Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor

Study Record Dates

First Submitted

March 7, 2025

First Posted

March 12, 2025

Study Start

March 20, 2025

Primary Completion

March 2, 2026

Study Completion

March 2, 2026

Last Updated

March 27, 2026

Record last verified: 2026-03

Locations

TU(1)