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Burden of urinary incontinence and sexual abnormalities on living standard in individuals suffering from spinal cord injury.

A cross- sectional study on the combined burden of bladder, bowel and sexual dysfunction as predictors of quality of life in individuals with chronic spinal cord injury - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/103903
Enrollment
80
Registered
2026-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G952- Other and unspecified cord compression

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: NIL: The participants will be assessed by using Neurogenic bowel dysfunction score for bowel difficulty, SCI-QOL

Sponsors

Amity Institute of Health Allied Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: individuals diagnosed with neurological level of injury of mid-thoracic T6 to T12 Lumbar L1 to L4 and Lumbo-sacral L5 to S1. Diagnosed with motor deficit according t the international standards for the neurological classification of SCI with an American spinal injury association impairment scale A to D. twelve months following the start of the spinal cord injury, post-acute rehabilitation was finished. married individuals diagnosed with bowel dysfunction with a minimum duration of six months with neurogenic bowel dysfunction score of 14 In case of female participants how many times a female have conceived? Willing to complete SCI-QOL bladder management difficulty Neurogenic bowel dysfunction score Integrated index for sexual function and WHO-QOL BREF

Exclusion criteria

Exclusion criteria: Acute or subacute SCI less than 12 months since injury severe cognitive impairment or psychiatric illness interfering with questionnaire completion Active severe medical illness that may affect the study participation Recent major pelvic bowel urological or genital surgery within the last 3 months Pregnant individuals Participation in another interventional study related to bladder bowel or sexual function

Design outcomes

Primary

MeasureTime frame
World health organization quality of life BREF versionTimepoint: At the baseline only i.e., on 1st day of assessment—

Secondary

MeasureTime frame
Spinal cord injury quality of life bladder management difficulty, Neurogenic bowel dysfunction score & integrated index of sexual function.Timepoint: One time study on the 1st day of meeting with the participants for 8 weeks—

Countries

India

Contacts

Public ContactDr Nidhi Sharma

Amity Institute of Health Allied Sciences

sharmanidhiphysio@gmail.com9760835605

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026