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Family Help Program: Nighttime Enuresis Treatment Program

I

IWK Health Centre

Status and phase

Completed
Phase 2

Conditions

Enuresis

Treatments

Behavioral: FHP Night time ENuresis Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT00270621
CIHR CAHR-43273
2234e

Details and patient eligibility

About

The purpose of the Strongest Families (formerly Family Help Program)is to evaluate the effectiveness of the Strongest Families distance intervention compared to usual or standard care that is typically provided to children with mild to moderate Enuresis diagnoses. This is a single-centre trial based at the IWK Health Centre. The primary outcome is change in diagnosis.

Full description

The purpose of the Family Help Program is to deliver, primary care mental health services to children and their families in the comfort and privacy of their own home. Approximately 46 children (5-12 years of age)suffering from pediatric enuresis (at least 2 times a week) will be randomized.

The intervention is delivered from a distance, using the urine alarm system accompanied by educational materials (manuals, video-tapes, audio-tapes) and telephone consultation with a trained paraprofessional "coach" who is supervised by a licensed health care professional. The telephone coach delivers consistent care based on written protocols, with on-going evaluation by a professional team.

Fifty percent of the eligible participants will receive Family Help Program telephone-based treatment and 50% will be referred back to their family physician to receive standard care as determined by that physician. Those receiving standard care will be evaluated for outcome results and then compared to the Family Help treated participants. It is anticipated that Family Help treatment will be proven to be as or more effective than standard care.

Enrollment

56 patients

Sex

All

Ages

5 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Is your child 3 to 12 years of age
  • child wets the bed more than twice per week
  • child dry during the day

Exclusion criteria

  • child received any treatment for bedwetting in the past 6 months
  • child at any time been dry for 6 months or longer
  • child currently on Imipramine or Desmopressin

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

56 participants in 2 patient groups

Treatment
Experimental group
Description:
FHP Night time Enuresis intervention
Treatment:
Behavioral: FHP Night time ENuresis Intervention
Control
No Intervention group
Description:
To receive standard/usual care for Nocturnal Enuresis- No FHP Night time Enuresis INtervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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