NCT07423624

Brief Summary

This randomized controlled trial examined the effects of a 12-week Zumba exercise program combined with halotherapy on body composition, aerobic capacity, and physical fitness parameters in adult women. Participants were randomly assigned to a Zumba plus halotherapy group or a control group. Physical fitness tests and body composition measurements were performed before and after the intervention.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

May 5, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2024

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 20, 2024

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

February 6, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

February 20, 2026

Completed
Last Updated

March 17, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

February 6, 2026

Last Update Submit

March 13, 2026

Conditions

Keywords

physical therapysedentary older adultsaerobic exerciseZumbahalotherapycomplementary therapypulmonary function

Outcome Measures

Primary Outcomes (3)

  • Body Composition

    Parameter: Body weight

    12 week

  • Aerobic Capacity

    Measured by \[ 6-minute walk test / VO₂max estimation\]

    12 weeks

  • Body Composition

    Parameter: BMI

    12 week

Secondary Outcomes (3)

  • Handgrip strength

    12 weeks

  • Flexibility

    12 weeks

  • Balance

    12 weeks

Study Arms (2)

Zumba + Halotherapy Group

EXPERIMENTAL

Participants performed Zumba training sessions \[haftada X gün, seans süresi\] for 12 weeks. Each session was followed by halotherapy exposure in a salt room environment.

Other: Zumba + Halotherapy GroupOther: Control

CONTROL

NO INTERVENTION

Participants maintained their usual daily activities without structured exercise or halotherapy.

Interventions

Participants performed Zumba training sessions \[haftada X gün, seans süresi\] for 12 weeks. Each session was followed by halotherapy exposure in a salt room environment.

Zumba + Halotherapy Group
ControlOTHER

Participants maintained their usual daily activities without structured exercise or halotherapy.

Zumba + Halotherapy Group

Eligibility Criteria

Age55 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Female participants aged \[55-80\] years
  • Sedentary or recreationally active
  • No regular exercise participation in the previous 6 months

You may not qualify if:

  • Cardiovascular, respiratory, or musculoskeletal disorders
  • Pregnancy
  • Participation in structured exercise programs during the study period

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gumushane Univetsity

Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, 29600, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
director

Study Record Dates

First Submitted

February 6, 2026

First Posted

February 20, 2026

Study Start

May 5, 2024

Primary Completion

August 15, 2024

Study Completion

August 20, 2024

Last Updated

March 17, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

The individual participant data collected in this study will not be shared with other researchers due to the need to protect participant confidentiality and the lack of permission for data sharing within the scope of informed consent.

Locations