NCT07764250

Brief Summary

older adults with mild and moderate cognitive impairment. compare immediate vs progressive standing dual-task training. assess balance, cognition, executive function, mobility, and quality of life.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
96

participants targeted

Target at P50-P75 for not_applicable

Timeline
0mo left

Started Jun 2026

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 Progress76%
Jun 2026Aug 2026

Study Start

First participant enrolled

June 25, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 9, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 13, 2026

Completed
12 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 25, 2026

Expected
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2026

Last Updated

August 13, 2026

Status Verified

August 1, 2026

Enrollment Period

2 months

First QC Date

August 9, 2026

Last Update Submit

August 9, 2026

Conditions

Keywords

CIMCIDTTISDTTPSDDT

Outcome Measures

Primary Outcomes (4)

  • MMSE

    4 WEEKS

  • MOCA

    4 WEEKS

  • TUG

    4 WEEKS

  • BBS

    4 WEEKS

Secondary Outcomes (2)

  • TMT

    4 WEEKS

  • QOL

    4 WEEKS

Study Arms (4)

ARM 1: Immediate Standing + Mild CI

EXPERIMENTAL
Other: Immediate standing dual task training

Arm 2: Progressive Standing + Mild CI

EXPERIMENTAL
Other: progressive standing dual task training

Arm 3 Immediate Standing + Moderate CI

EXPERIMENTAL
Other: Immediate standing dual task training

Arm 4 Progressive Standing + Moderate CI

EXPERIMENTAL
Other: progressive standing dual task training

Interventions

Motor-cognitive dual-task training is a rehabilitation intervention delivered by a physiotherapist over 8 weeks, with three sessions per week, each lasting 45 minutes. Every session consists of a 5-minute warm-up, 30-35 minutes of dual-task training, and a 5-minute cool-down. It simultaneously combines motor and cognitive tasks. Motor components include marching in place, finger tapping, hand transfer activities, side stepping, weight shifting, heel raises, heel-toe stepping, and balance challenges. Cognitive components include naming animals or fruits, counting forward, and months, serial subtraction by threes, backward digit span, alternate naming, and word recall. Participants allocated to the Immediate Standing intervention perform all dual-task activities in standing from the first treatment session.

Also known as: progressive standing dual task training
ARM 1: Immediate Standing + Mild CIArm 3 Immediate Standing + Moderate CI

Motor-cognitive dual-task training is a rehabilitation intervention delivered by a physiotherapist over 8 weeks, with three sessions per week, each lasting 45 minutes. Every session consists of a 5-minute warm-up, 30-35 minutes of dual-task training, and a 5-minute cool-down. It simultaneously combines motor and cognitive tasks. Motor components include marching in place, finger tapping, hand transfer activities, side stepping, weight shifting, heel raises, heel-toe stepping, and balance challenges. Cognitive components include naming animals or fruits, counting forward, and months, serial subtraction by threes, backward digit span, alternate naming, and word recall. Participants allocated to the Progressive Standing intervention initially perform dual-task activities sitting and progressively transition to standing during the intervention period.

Arm 2: Progressive Standing + Mild CIArm 4 Progressive Standing + Moderate CI

Eligibility Criteria

Age55 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age ≥55 years Mild or moderate cognitive impairment MoCA 10-25 MMSE 10-23 Able to participate Provides informed consent

You may not qualify if:

  • Severe cognitive impairment Severe sensory or musculoskeletal impairments Unstable medical conditions Participation in another intervention study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pakistan institute of medical sciences

Islamabad, Capital, Pakistan

RECRUITING

MeSH Terms

Conditions

Cognitive Dysfunction

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized Control Trial (RCT)
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

August 9, 2026

First Posted

August 13, 2026

Study Start

June 25, 2026

Primary Completion (Estimated)

August 25, 2026

Study Completion (Estimated)

August 30, 2026

Last Updated

August 13, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations