HIT-MMEX: High Intensity Multi-Modal Exercise Training in Postmenopausal Women

Sponsor
Riphah International University (Other)
Overall Status
Completed
CT.gov ID
NCT04653350
Collaborator
(none)
58
2
2
19.3
29
1.5

Study Details

Study Description

Brief Summary

in Pakistan 9.9 million people are osteoporotic and 7.2 million amongst them are women. Globally after every 3 seconds there is occurrence of fragility fracture.In Pakistan females carries different risk factors based on distinct culture, environment, diet and lifestyle. So there is dire need to conduct more high quality clinical trials at National level in order to establish strong evidence in favor of low cost but highly effective exercise protocols for such a significant public health issue.

Condition or Disease Intervention/Treatment Phase
  • Other: High Intensity Exercises
  • Other: General Exercises
N/A

Detailed Description

In postmenopausal age, women bones get weak and easily fracture after 50years. In Pakistan every other female is silently suffering from this disease leading to bone, joint pain and disability. This project is innovatively designed first time in Pakistan to target weak bones of women with high intensity, progressive exercise training. The objectives of this study are to determine the effects of a high intensity multi-modal exercise training on bone mineral density and functional performance in postmenopausal women.

After initial screening based on history, subjective fracture risk calculations and subjective osteoporosis screening. Females fulfilling criteria and willing to participate in exercise trial will be recruited in the study. At baseline, DEXA scan will be done for Femoral and lumbar bone density. All performance based testing for functional performance outcome measures would be done at baseline, after 3 months & after 6 months. Patient will be called twice a week for 8months and DEXA will be repeated after 8months of training. It is hypothesized that supervised exercise training will improve bone mineral density and functional performance in postmenopausal women with low bone mass.

Study Design

Study Type:
Interventional
Actual Enrollment :
58 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This will be a Single factor, Pretest-Postest Control group Design with parallel assignment of patients into two groups.This will be a Single factor, Pretest-Postest Control group Design with parallel assignment of patients into two groups.
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Females participating in a clinical trial will be kept blind with respect to their allocated exercise group. The assessor doing reporting for the DEXA scan will also be kept blind about the patient group.
Primary Purpose:
Treatment
Official Title:
Effects of High Intensity Multi-Modal Exercise Training on Bone Density and Functional Performance in Postmenopausal Women
Actual Study Start Date :
Nov 1, 2020
Actual Primary Completion Date :
Jun 10, 2022
Actual Study Completion Date :
Jun 10, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: HIT-MMEX Group

In this group Supervised High intensity Progressive Resistance Training, High intensity weightbearing/Impact exercises and High challenging Balance Training will be given. 2 times/week for 40-50minutes session progressively over the duration of 8 months.

Other: High Intensity Exercises
Supervised High intensity Progressive Resistance Training, High intensity weightbearing/Impact exercises and High challenging Balance Training will be given. 2 times/week for 40-50minutes session progressively over the duration of 8 months.

Active Comparator: Control Group

In this Group Supervised general fitness exercises including general body stretches, treadmill walking, mild to moderate intensity progressive resistance training & balance exercises will be given. 2 times/week for 40-50minutes session progressively over the duration of 8 months.

Other: General Exercises
Supervised general fitness exercises including general body stretches, treadmill walking, mild to moderate intensity progressive resistance training & balance exercises will be given. 2 times/week for 40-50minutes session progressively over the duration of 8 months

Outcome Measures

Primary Outcome Measures

  1. Femoral Neck BMD (FN BMD) [8 Months]

    Change from Baseline in Femoral Neck Bone Mineral Density measured by DEXA scan

  2. Lumbar Spine BMD (LS BMD) [8 Months]

    Change from Baseline in Lumbar Spine Bone Mineral Density measured by DEXA scan

Secondary Outcome Measures

  1. 1 RM for Leg Extensors [3 Months]

    Changes from the baseline, 1 RM Is used to assess maximum muscle strength. Patient will be asked to perform leg press that is to extend knee against maximum resistance once. weight will be recorded in Kgs.

  2. 1 RM for Leg Extensors [6 Months]

    Changes from 3 Months, 1 RM Is used to assess maximum muscle strength. Patient will be asked to perform leg press that is to extend knee against maximum resistance once. weight will be recorded in Kgs.

  3. 1 RM for Trunk Extensors [3 Months]

    Changes Baseline, 1 RM Is used to assess maximum muscle strength. Patient will be asked to perform deadlift, maximum weight lifted will be recorded in Kgs.

  4. 1 RM for Trunk Extensors [6 Months]

    Changes from 3 Months, 1 RM Is used to assess maximum muscle strength. Patient will be asked to perform deadlift, maximum weight lifted will be recorded in Kgs.

  5. 30-second sit to stand test (Reps) [3 Months]

    Changes from Baseline, It involves counting the number of times the participant can rise to a full standing position from the seated position on a chair without using the arms

  6. 30-second sit to stand test (Reps) [6 Months]

    Changes from 3 Months, It involves counting the number of times the participant can rise to a full standing position from the seated position on a chair without using the arms

  7. Time up and Go test [3 Months]

    Changes from Baseline, participants will be instructed to walk at usual speed for three meter and then walk back to sit down .Note time on stopwatch .The average of tests trail will be measured as the mean of TUG.

  8. Time up and Go test [6 Months]

    Changes from 3 Months, participants will be instructed to walk at usual speed for three meter and then walk back to sit down .Note time on stopwatch .The average of tests trail will be measured as the mean of TUG.

  9. Dynamic Gait Index [3 Months]

    Changes from Baseline, DGI was Developed to assess the likelihood of falling in older adults. Designed to test eight facets of gait. A four-point ordinal scale, ranging from 0-3. "0" indicates the lowest level of function and "3" the highest level of function. Total Score is 24

  10. Dynamic Gait Index [6 Months]

    Changes from 3 months, DGI was Developed to assess the likelihood of falling in older adults. Designed to test eight facets of gait. A four-point ordinal scale, ranging from 0-3. "0" indicates the lowest level of function and "3" the highest level of function. Total Score is 24

  11. Falls Efficacy Scale [3 Months]

    Changes from Baseline, On a scale from 1 to 10, with 1 being very confident and 10 being not confident at all, patient will be asked how confident are you that you do the given activities without falling. A total score of greater than 70 indicates that the person has a fear of falling.

  12. Falls Efficacy Scale [6 Months]

    Changes from 3Months, On a scale from 1 to 10, with 1 being very confident and 10 being not confident at all, patient will be asked how confident are you that you do the given activities without falling. A total score of greater than 70 indicates that the person has a fear of falling.

  13. Berg balance scale [3 Months]

    Changes from Baseline, The Berg balance scale is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function and takes approximately 20 minutes to complete. It does not include the assessment of gait.

  14. Berg balance scale [6 Months]

    Changes from 3Months, The Berg balance scale is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function and takes approximately 20 minutes to complete. It does not include the assessment of gait.

  15. Functional Reach Test (FRT) [3 Months]

    Changes from Baseline, it is a clinical outcome measure and assessment tool for ascertaining dynamic balance in one simple task.In standing, measures the distance between the length of an outstretched arm in a maximal forward reach, while maintaining a fixed base of support.

  16. Functional Reach Test (FRT) [6 Months]

    Changes from 3 months, it is a clinical outcome measure and assessment tool for ascertaining dynamic balance in one simple task.In standing, measures the distance between the length of an outstretched arm in a maximal forward reach, while maintaining a fixed base of support.

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years to 70 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Postmenopausal Women, at least 3 years since last mensuration.

  • Age: 45-70years

  • Body mass index (BMI) <30kg/m2

  • Community ambulant without walking aid

  • Good general health

  • Willing for exercise therapy

Exclusion Criteria:
  • History of fragility fracture in addition to BMD T-score of -2.5 or less

  • MMSE < 20

  • Taking Hormone replacement therapy or steroids from last 1 year.

  • Had participated in regular exercise for last 1 year

  • Systemic illness: hyperthyroidism, hyperparathyroidism, Diabetes Mellitus, renal failure, any malignancy, extensive radiation exposure

  • Any orthopedic injury/disorder hindering performance of exercise.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rehab Center RCRAHS Potohar campus Rawalpindi Punjab Pakistan 40100
2 Behbud Association of Pakistan Rawalpindi Punjab Pakistan 46000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Huma Riaz, Phd*, Riphah International University
  • Study Chair: Muhammad Naveed Babur, Phd, Isra University islamabad

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Huma Riaz, Associate Professor, Riphah International University
ClinicalTrials.gov Identifier:
NCT04653350
Other Study ID Numbers:
  • RiphahIU Huma Riaz
First Posted:
Dec 4, 2020
Last Update Posted:
Jun 21, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 21, 2022