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CompletedNCT04213339Updated Jul 28, 2020

Effectiveness of Kegal Exercises on Urinary Incontinence Impact in Geriatric Incontinence

An interventional study of Kegel Exercises in Urinary Incontinence in Geriatric Population, sponsored by Zohra Institute of Health Sciences. Completed at 1 site in Pakistan. Open to male participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2020-07-28.

Sponsored by Zohra Institute of Health Sciences · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
50 Years to 80 Years
Sex
Male
01

Study summary

This research study was used to determine effectiveness of kegal exercise on urinary incontinence impact in geriatric incontinence. There were two groups, One group was experimental which was subjected to Kegel exercises while other was control group without any treatment.

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Conditions studied

  • Urinary Incontinence in Geriatric Population
03

In context

Urinary Incontinence

1,363 studies on the registry are indexed under Urinary Incontinence; 228 are open to participants now.

This study's enrollment of 50 is below the median of 66 across 1,011 interventional studies indexed under Urinary Incontinence.

Browse Urinary Incontinence studies →

Lead sponsor

Zohra Institute of Health Sciences is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 80 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Patient 50 years of age and above.
  • Geriatric population
  • Male participant

Exclusion criteria

Exclusion Criteria:

  • Patient below 50 years of age.
  • Patient with neurological problem.
  • Uncooperative attitude
  • Male patients with prostate problem \& Female participants
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    Kegal Exercises

    Behavioral: Kegel Exercises

  • No intervention
    Control

Interventions

  • BehavioralKegel Exercises

    Kegel exercise group will get exercise within duration of 3 to 6 weeks based on age factor. Kegel exercise can be performed at any time and at any place without any restrictions. following steps will be followed by kegel exercises group members: 1. Tighten and hold pelvic floor muscles for five seconds (count 1 one thousand, 2 one thousand, 3 one thousand, 4 one thousand, 5 one thousand). 2. Relax pelvic muscles and perform 10 to 20 Kegel exercises three to four times each day. 3. Squeeze the muscles in anus like holding a bowel movement focus penile area 4. Relax the pelvic floor muscles after each attempt. 5. Repeat this exercise 10 to 20 times. 6. While performing Kegel exercises: Do not hold the breath. Do not push down. Squeeze the muscles together tightly and imagine, trying to lift this muscle up. Do not tighten the muscles in the stomach, buttocks, or thighs. While the control group did not participate in any kegel exercises

06

What researchers measure

Primary outcomes

  1. Incontinence Impact

    Incontinence impact questionnaire description: For each question, circle the response that best describes how much your activities, relationships, and feelings are being affected by urine leakage. Scoring: Items 1 and 2 = physical activity Items 3 and 4 = travel Item 5 = social/relationships Items 6 and 7 = emotional health Scoring. Item responses are assigned values of 0 for "not at all," 1 for "slightly," 2 for "moderately," and 3 for "greatly." The average score of items responded to is calculated. The average, which ranges from 0 to 3, is multiplied by 33 1/3 to put scores on a scale of 0 to 100. 1. Ability to do household chores 2. Physical recreation such as walking, swimming, or other exercise? 3. Entertainment activities 4. Ability to travel by car or bus more than 30 minutes from home. 5. Participation in social activities outside your home 6. Emotional health 7. Feeling frustrated?

    Time frame: 6 to 8 weeks

07

Study locations

1 site
  • Ali Sikandar Bhutto
    Rawalpindi, Pakistan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 28, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04213339
Lead sponsor
Zohra Institute of Health Sciences
Responsible party
Suhail Karim (Assistant Professor, Riphah International University) — Principal investigator
First posted
Dec 30, 2019
Start date
Jan 3, 2020
Primary completion
May 28, 2020
Completion
Jun 30, 2020
Last update
Jul 28, 2020

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2020. You cannot join it, but the record below documents what was studied.

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