NCT07138911

Brief Summary

To evaluate the effect of home-based exercise plan mediated by a digital health application on kinesiophobia and functional capacity in sedentary post myocardial infarction patients. Evidence suggest that digital health application significantly improve physical activity level in patient following cardiac event by providing personalized exercise plan, real time feed back, progress tracking and motivational features which enhanced adherence and engagement in rehabilitation program. This study could offer a viable le solution for overcoming barrier to rehabilitation particularly for those unable to access traditional clinic-based program

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
88

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 13, 2025

Completed
5 days until next milestone

First Submitted

Initial submission to the registry

August 18, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 24, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2026

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 25, 2026

Completed
Last Updated

February 25, 2026

Status Verified

February 1, 2026

Enrollment Period

6 months

First QC Date

August 18, 2025

Last Update Submit

February 23, 2026

Conditions

Myocardial InfarctionKinesiophobiaSedentary Behavior

Keywords

Digital health appFunctional capacityKinesiophobiaMyocardial InfarctionSedentary

Outcome Measures

Primary Outcomes (2)

  • Kinesiophobia

    Changes from baseline to 4 weeks after intervention, measured through the TSK-SV Heart specifically focuses on assessing Kinesiophobia in the context of cardiac conditions or symptoms. It include questions related to fear of engaging in physical activity due to concerns about cardiac events (such as heart palpitations, chest pain, or shortness of breath) during exercise or daily activities. The 17 item TSK total scores range from 17 to 68 where the lowest 17 means no or negligible Kinesiophobia, and the higher scores indicate an increasing degree of Kinesiophobia.

    4 Weeks

  • Functional Capacity

    Changes from baseline to 4 weeks after intervention, measured through six minute walk test which is a sub-maximal exercise test used to assess functional capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity.

    4 Weeks

Study Arms (2)

Intervention group

EXPERIMENTAL

Home based exercise plan mediated by use of mobile health app

Other: Intervention group

Control Group

ACTIVE COMPARATOR

Home based exercise plan

Other: Control group

Interventions

Intervention groupOTHER

Walking at home for 15-30 minutes 3 times per day for 4 weeks. Activity plan is calendar on mobile health app. Mobile placed in pocket or bag before starting walk and mark activity on calendar.

Intervention group
Control groupOTHER

Walking at home for 15-30 minutes 3 times per day for 4 weeks. Manual record of walking and date.

Control Group

Eligibility Criteria

Age30 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • months post myocardial infarction patient
  • Sitting hours \>8
  • IPAQ \< 600 Mets minutes

You may not qualify if:

  • Unstable Angina
  • Recurrent Myocardial infarction
  • Recent surgery or Procedure
  • Heart failure, Arrhythmia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Polyclinic Hospital

Islamabad, Federal, 45300, Pakistan

RECRUITING

MeSH Terms

Conditions

Myocardial InfarctionKinesiophobiaSedentary Behavior

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosisPhobic DisordersAnxiety DisordersMental DisordersBehavior

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Officials

  • Mehwish Waseem, MS-CPPT PhD*

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Mehwish Waseem, MS-CPPT PhD*

CONTACT

0331-5309015mehwish.waseem@riphah.edu.pk

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 18, 2025

First Posted

August 24, 2025

Study Start

August 13, 2025

Primary Completion

February 20, 2026

Study Completion

February 25, 2026

Last Updated

February 25, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Locations

PA(1)